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<!--
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UID=311052
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ConceptID=C1709246
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-->
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<!--imgCountBooks = 0--><h1 class="medgenTitle"><div class="MedGenTitleText">Non-Neoplastic Disorder</div></h1><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>311052</dd><dt><span class="dotprefix"> •</span>Concept ID: </dt><dd><a href="/medgen/docs/help/#sources" target="_blank" title="Concept Unique Identifier from NLM's Unified Medical Language system (UMLS) Click for more information.">C1709246</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div><table class="medgenTable"><tbody><tr><td>Synonym:</td>
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<td>Non-Neoplastic Disease</td></tr>
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<div class="portlet_head mgSectionHead ui-widget-header"><h1 class="nl" id="Definition">Definition</h1><a sid="100" href="#" class="portlet_shutter" title="Show/hide content"></a></div>
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<div class="portlet_content ln">Any disorder other than abnormal tissue growth resulting from uncontrolled cell proliferation. [from <a title="NCI Thesaurus" href="http://ncit.nci.nih.gov" class="defSource" target="_blank">NCI</a>]</div>
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<div class="portlet_head mgSectionHead ui-widget-header"><h1 class="nl" id="Term_Hierarchy">Term Hierarchy</h1><a sid="118" href="#" class="portlet_shutter" title="Show/hide content"></a></div>
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<div class="portlet_content ln HierarchyGTR"><div class="jig-ncbitabs"><ul><li><a href="#tabGTR">GTR</a></li><li><a href="#tabMGEN">MeSH</a></li></ul><div id="tabGTR"><div class="search_result"><div class="rprts"><div class="chiclet_legend"><span class="chiclet_list" style="position:static;"><span title="Clinical test" class="chiclet Ccolor round">C</span><span>Clinical test, </span><span title="Research test" class="chiclet Rcolor round">R</span><span>Research test, </span><span title="OMIM" class="chiclet Ocolor ">O</span><span>OMIM, </span><span title="GeneReview" class="chiclet Gcolor">G</span><span><em>GeneReviews</em>, </span><span title="ClinVar" class="chiclet Vcolor">V</span><span>ClinVar </span></span></div><div id="hierarchy" class="margin_t1"><div class="ds_tree"><ul><li class="matched_ds"><span class="chiclet_list"><span class="chiclet unavailable round" title="Clinical test">C</span><span class="chiclet unavailable round" title="Research Tests">R</span><span class="chiclet unavailable" title="OMIM">O</span><span class="chiclet unavailable" title="GeneReviews">G</span><span class="chiclet unavailable" title="ClinVar">V</span></span><span class="TLline">Non-Neoplastic Disorder</span></li></ul></div></div></div></div></div><div id="tabMGEN"><div class="ds_tree"><ul><li><span class="TLline"><a href="/medgen/21047" ref="tree=MeSH" title="MedGen record for Pathological Conditions, Signs and Symptoms">Pathological Conditions, Signs and Symptoms</a></span><ul><li><span class="TLline"><a href="/medgen/18325" ref="tree=MeSH" title="MedGen record for Pathological process">Pathological process</a></span><ul><li><span class="TLline"><a href="/medgen/4347" ref="tree=MeSH" title="MedGen record for Disease">Disease</a></span><ul><li><span class="matched_ds">Non-Neoplastic Disorder</span><ul><li><span class="TLline"><a href="/medgen/353985" ref="tree=MeSH" title="MedGen record for Non-Neoplastic Disorder by Site">Non-Neoplastic Disorder by Site</a></span><ul><li><span class="TLline"><a href="/medgen/233231" ref="tree=MeSH" title="MedGen record for Non-Neoplastic Breast Disorder">Non-Neoplastic Breast Disorder</a></span><ul><li><span class="TLline"><a href="/medgen/1744840" ref="tree=MeSH" title="MedGen record for Atypical Vascular Lesion of Breast">Atypical Vascular Lesion of Breast</a></span></li><li><span class="TLline"><a href="/medgen/39336" ref="tree=MeSH" title="MedGen record for Breast adenosis">Breast adenosis</a></span></li><li><span class="TLline"><a href="/medgen/42015" ref="tree=MeSH" title="MedGen record for Breast fibrocystic disease">Breast fibrocystic disease</a></span></li><li><span class="TLline"><a href="/medgen/116039" ref="tree=MeSH" title="MedGen record for Breast Hamartoma">Breast Hamartoma</a></span></li><li><span class="TLline"><a href="/medgen/43789" ref="tree=MeSH" title="MedGen record for Breast hypertrophy">Breast hypertrophy</a></span></li><li><span class="TLline"><a href="/medgen/75594" ref="tree=MeSH" title="MedGen record for Breast hypoplasia">Breast hypoplasia</a></span></li><li><span class="TLline"><a href="/medgen/57847" ref="tree=MeSH" title="MedGen record for Fat necrosis of breast">Fat necrosis of breast</a></span></li><li><span class="TLline"><a href="/medgen/6694" ref="tree=MeSH" title="MedGen record for Gynecomastia">Gynecomastia</a></span></li><li><span class="TLline"><a href="/medgen/5997" ref="tree=MeSH" title="MedGen record for Lactation disease">Lactation disease</a></span></li><li><span class="TLline"><a href="/medgen/101829" ref="tree=MeSH" title="MedGen record for Lactocele">Lactocele</a></span></li><li><span class="TLline"><a href="/medgen/57538" ref="tree=MeSH" title="MedGen record for Mammary duct ectasia">Mammary duct ectasia</a></span></li><li><span class="TLline"><a href="/medgen/9901" ref="tree=MeSH" title="MedGen record for Mastitis">Mastitis</a></span></li></ul></li><li><span class="TLline"><a href="/medgen/233232" ref="tree=MeSH" title="MedGen record for Non-Neoplastic Cardiovascular Disorder">Non-Neoplastic Cardiovascular Disorder</a></span><ul><li><span class="TLline"><a href="/medgen/777090" ref="tree=MeSH" title="MedGen record for Arteriosclerotic Cardiovascular Disease">Arteriosclerotic Cardiovascular Disease</a></span></li><li><span class="TLline"><a href="/medgen/2039" ref="tree=MeSH" title="MedGen record for Cardiac arrhythmia">Cardiac arrhythmia</a></span></li><li><span class="TLline"><a href="/medgen/777113" ref="tree=MeSH" title="MedGen record for Congenital anomaly of cardiovascular system">Congenital anomaly of cardiovascular system</a></span></li><li><span class="TLline"><a href="/medgen/277425" ref="tree=MeSH" title="MedGen record for Non-Neoplastic Heart Disorder">Non-Neoplastic Heart Disorder</a></span></li><li><span class="TLline"><a href="/medgen/233247" ref="tree=MeSH" title="MedGen record for Non-Neoplastic Vascular Disorder">Non-Neoplastic Vascular Disorder</a></span></li><li><span class="TLline"><a href="/medgen/65965" ref="tree=MeSH" title="MedGen record for Pulmonary artery stenosis">Pulmonary artery stenosis</a></span></li></ul></li><li><span class="TLline"><a href="/medgen/277424" ref="tree=MeSH" title="MedGen record for Non-Neoplastic Connective and Soft Tissue Disorder">Non-Neoplastic Connective and Soft Tissue Disorder</a></span><ul><li><span class="TLline"><a href="/medgen/7190" ref="tree=MeSH" title="MedGen record for Arthropathy">Arthropathy</a></span></li><li><span class="TLline"><a href="/medgen/411197" ref="tree=MeSH" title="MedGen record for Juvenile hyaline fibromatosis">Juvenile hyaline fibromatosis</a></span></li><li><span class="TLline"><a href="/medgen/1716265" ref="tree=MeSH" title="MedGen record for Non-Neoplastic Musculoskeletal Disorder">Non-Neoplastic Musculoskeletal Disorder</a></span></li><li><span class="TLline"><a href="/medgen/233244" ref="tree=MeSH" title="MedGen record for Non-Neoplastic Soft Tissue Disorder">Non-Neoplastic Soft Tissue Disorder</a></span></li></ul></li><li><span class="TLline"><a href="/medgen/233773" ref="tree=MeSH" title="MedGen record for Non-Neoplastic Digestive System Disorder">Non-Neoplastic Digestive System Disorder</a></span><ul><li><span class="TLline"><a href="/medgen/473237" ref="tree=MeSH" title="MedGen record for Congenital Digestive System Disorder">Congenital Digestive System Disorder</a></span></li><li><span class="TLline"><a href="/medgen/675852" ref="tree=MeSH" title="MedGen record for Infectious disease of digestive tract">Infectious disease of digestive tract</a></span></li><li><span class="TLline"><a href="/medgen/311051" ref="tree=MeSH" title="MedGen record for Non-Neoplastic Anal Disorder">Non-Neoplastic Anal Disorder</a></span></li><li><span class="TLline"><a href="/medgen/1721923" ref="tree=MeSH" title="MedGen record for Non-Neoplastic Appendix Disorder">Non-Neoplastic Appendix Disorder</a></span></li><li><span class="TLline"><a href="/medgen/317956" ref="tree=MeSH" title="MedGen record for Non-Neoplastic Esophageal Disorder">Non-Neoplastic Esophageal Disorder</a></span></li><li><span class="TLline"><a href="/medgen/474713" ref="tree=MeSH" title="MedGen record for Non-Neoplastic Hepatobiliary Disorder">Non-Neoplastic Hepatobiliary Disorder</a></span></li><li><span class="TLline"><a href="/medgen/364129" ref="tree=MeSH" title="MedGen record for Non-Neoplastic Intestinal Disorder">Non-Neoplastic Intestinal Disorder</a></span></li><li><span class="TLline"><a href="/medgen/317959" ref="tree=MeSH" title="MedGen record for Non-Neoplastic Pancreatic Disorder">Non-Neoplastic Pancreatic Disorder</a></span></li><li><span class="TLline"><a href="/medgen/364130" ref="tree=MeSH" title="MedGen record for Non-Neoplastic Stomach Disorder">Non-Neoplastic Stomach Disorder</a></span></li><li><span class="TLline"><a href="/medgen/45384" ref="tree=MeSH" title="MedGen record for Peptic ulcer">Peptic ulcer</a></span></li></ul></li><li><span class="TLline"><a href="/medgen/233771" ref="tree=MeSH" title="MedGen record for Non-Neoplastic Endocrine Disorder">Non-Neoplastic Endocrine Disorder</a></span><ul><li><span class="TLline"><a href="/medgen/777159" ref="tree=MeSH" title="MedGen record for 11-Beta-Hydroxylase Deficiency">11-Beta-Hydroxylase Deficiency</a></span></li><li><span class="TLline"><a href="/medgen/1372371" ref="tree=MeSH" title="MedGen record for 17-Alpha-Hydroxylase/17,20 Lyase Deficiency">17-Alpha-Hydroxylase/17,20 Lyase Deficiency</a></span></li><li><span class="TLline"><a href="/medgen/468578" ref="tree=MeSH" title="MedGen record for 21-Hydroxylase Deficiency">21-Hydroxylase Deficiency</a></span></li><li><span class="TLline"><a href="/medgen/452446" ref="tree=MeSH" title="MedGen record for 3 beta-Hydroxysteroid dehydrogenase deficiency">3 beta-Hydroxysteroid dehydrogenase deficiency</a></span></li><li><span class="TLline"><a href="/medgen/589758" ref="tree=MeSH" title="MedGen record for Adrenal cortical hypofunction">Adrenal cortical hypofunction</a></span></li><li><span class="TLline"><a href="/medgen/453383" ref="tree=MeSH" title="MedGen record for Atrophy of thyroid">Atrophy of thyroid</a></span></li><li><span class="TLline"><a href="/medgen/39042" ref="tree=MeSH" title="MedGen record for Autoimmune polyendocrinopathy">Autoimmune polyendocrinopathy</a></span></li><li><span class="TLline"><a href="/medgen/272506" ref="tree=MeSH" title="MedGen record for Congenital Adrenal Gland Disorder">Congenital Adrenal Gland Disorder</a></span></li><li><span class="TLline"><a href="/medgen/208865" ref="tree=MeSH" title="MedGen record for Congenital Thyroid Gland Disorder">Congenital Thyroid Gland Disorder</a></span></li><li><span class="TLline"><a href="/medgen/8349" ref="tree=MeSH" title="MedGen record for Diabetes insipidus">Diabetes insipidus</a></span></li><li><span class="TLline"><a href="/medgen/858942" ref="tree=MeSH" title="MedGen record for Disorder of AMH">Disorder of AMH</a></span></li><li><span class="TLline"><a href="/medgen/858943" ref="tree=MeSH" title="MedGen record for Disorder of AMH Receptor">Disorder of AMH Receptor</a></span></li><li><span class="TLline"><a href="/medgen/890363" ref="tree=MeSH" title="MedGen record for Disorder of Androgen Synthesis">Disorder of Androgen Synthesis</a></span></li><li><span class="TLline"><a href="/medgen/56342" ref="tree=MeSH" title="MedGen record for Endocrine Disorder Arising from Mental Factor">Endocrine Disorder Arising from Mental Factor</a></span></li><li><span class="TLline"><a href="/medgen/226229" ref="tree=MeSH" title="MedGen record for Glucose metabolism disease">Glucose metabolism disease</a></span></li><li><span class="TLline"><a href="/medgen/42270" ref="tree=MeSH" title="MedGen record for Goiter">Goiter</a></span></li><li><span class="TLline"><a href="/medgen/181797" ref="tree=MeSH" title="MedGen record for Gonadal agenesis">Gonadal agenesis</a></span></li><li><span class="TLline"><a href="/medgen/1372270" ref="tree=MeSH" title="MedGen record for Hyperandrogenism due to cortisone reductase deficiency">Hyperandrogenism due to cortisone reductase deficiency</a></span></li><li><span class="TLline"><a href="/medgen/6972" ref="tree=MeSH" title="MedGen record for Hyperthyroidism">Hyperthyroidism</a></span></li><li><span class="TLline"><a href="/medgen/5711" ref="tree=MeSH" title="MedGen record for Hypogonadism">Hypogonadism</a></span></li><li><span class="TLline"><a href="/medgen/6985" ref="tree=MeSH" title="MedGen record for Hypoparathyroidism">Hypoparathyroidism</a></span></li><li><span class="TLline"><a href="/medgen/9386" ref="tree=MeSH" title="MedGen record for Hypopituitarism">Hypopituitarism</a></span></li><li><span class="TLline"><a href="/medgen/6991" ref="tree=MeSH" title="MedGen record for Hypothyroidism">Hypothyroidism</a></span></li><li><span class="TLline"><a href="/medgen/390686" ref="tree=MeSH" title="MedGen record for Mullerian aplasia and hyperandrogenism">Mullerian aplasia and hyperandrogenism</a></span></li><li><span class="TLline"><a href="/medgen/215300" ref="tree=MeSH" title="MedGen record for Pituitary gland hypoplasia">Pituitary gland hypoplasia</a></span></li><li><span class="TLline"><a href="/medgen/46178" ref="tree=MeSH" title="MedGen record for Pseudohypoparathyroidism">Pseudohypoparathyroidism</a></span></li><li><span class="TLline"><a href="/medgen/116061" ref="tree=MeSH" title="MedGen record for Pyknodysostosis">Pyknodysostosis</a></span></li><li><span class="TLline"><a href="/medgen/120626" ref="tree=MeSH" title="MedGen record for Testosterone 17-beta-dehydrogenase deficiency">Testosterone 17-beta-dehydrogenase deficiency</a></span></li><li><span class="TLline"><a href="/medgen/21548" ref="tree=MeSH" title="MedGen record for Thyroiditis">Thyroiditis</a></span></li><li><span class="TLline"><a href="/medgen/21734" ref="tree=MeSH" title="MedGen record for Turner syndrome">Turner syndrome</a></span></li></ul></li><li><span class="TLline"><a href="/medgen/235381" ref="tree=MeSH" title="MedGen record for Non-Neoplastic Eye Disorder">Non-Neoplastic Eye Disorder</a></span><ul><li><span class="TLline"><a href="/medgen/57702" ref="tree=MeSH" title="MedGen record for Amaurosis fugax">Amaurosis fugax</a></span></li><li><span class="TLline"><a href="/medgen/598" ref="tree=MeSH" title="MedGen record for Blepharitis">Blepharitis</a></span></li><li><span class="TLline"><a href="/medgen/2669" ref="tree=MeSH" title="MedGen record for Blepharoconjunctivitis">Blepharoconjunctivitis</a></span></li><li><span class="TLline"><a href="/medgen/39462" ref="tree=MeSH" title="MedGen record for Cataract">Cataract</a></span></li><li><span class="TLline"><a href="/medgen/944" ref="tree=MeSH" title="MedGen record for Choroideremia">Choroideremia</a></span></li><li><span class="TLline"><a href="/medgen/4623" ref="tree=MeSH" title="MedGen record for Congenital anomaly of eye">Congenital anomaly of eye</a></span></li><li><span class="TLline"><a href="/medgen/1046" ref="tree=MeSH" title="MedGen record for Congenital ocular coloboma">Congenital ocular coloboma</a></span></li><li><span class="TLline"><a href="/medgen/266257" ref="tree=MeSH" title="MedGen record for Contact lens overwear syndrome">Contact lens overwear syndrome</a></span></li><li><span class="TLline"><a href="/medgen/41372" ref="tree=MeSH" title="MedGen record for Cyclitis">Cyclitis</a></span></li><li><span class="TLline"><a href="/medgen/87432" ref="tree=MeSH" title="MedGen record for Disorder of eye due to diabetes mellitus">Disorder of eye due to diabetes mellitus</a></span></li><li><span class="TLline"><a href="/medgen/4411" ref="tree=MeSH" title="MedGen record for Dry eye syndrome">Dry eye syndrome</a></span></li><li><span class="TLline"><a href="/medgen/41934" ref="tree=MeSH" title="MedGen record for Eye infectious disease">Eye infectious disease</a></span></li><li><span class="TLline"><a href="/medgen/858747" ref="tree=MeSH" title="MedGen record for Fat Adherence Syndrome">Fat Adherence Syndrome</a></span></li><li><span class="TLline"><a href="/medgen/42224" ref="tree=MeSH" title="MedGen record for Glaucoma">Glaucoma</a></span></li><li><span class="TLline"><a href="/medgen/9379" ref="tree=MeSH" title="MedGen record for Hyphema">Hyphema</a></span></li><li><span class="TLline"><a href="/medgen/853096" ref="tree=MeSH" title="MedGen record for Intraocular Lens Dislocation">Intraocular Lens Dislocation</a></span></li><li><span class="TLline"><a href="/medgen/7160" ref="tree=MeSH" title="MedGen record for Iritis">Iritis</a></span></li><li><span class="TLline"><a href="/medgen/44014" ref="tree=MeSH" title="MedGen record for Keratoconjunctivitis">Keratoconjunctivitis</a></span></li><li><span class="TLline"><a href="/medgen/6043" ref="tree=MeSH" title="MedGen record for Lens luxation">Lens luxation</a></span></li><li><span class="TLline"><a href="/medgen/235379" ref="tree=MeSH" title="MedGen record for Non-Neoplastic Conjunctival Disorder">Non-Neoplastic Conjunctival Disorder</a></span></li><li><span class="TLline"><a href="/medgen/235380" ref="tree=MeSH" title="MedGen record for Non-Neoplastic Corneal Disorder">Non-Neoplastic Corneal Disorder</a></span></li><li><span class="TLline"><a href="/medgen/235382" ref="tree=MeSH" title="MedGen record for Non-Neoplastic Eyelid Disorder">Non-Neoplastic Eyelid Disorder</a></span></li><li><span class="TLline"><a href="/medgen/1784225" ref="tree=MeSH" title="MedGen record for Non-Neoplastic Lacrimal System Disorder">Non-Neoplastic Lacrimal System Disorder</a></span></li><li><span class="TLline"><a href="/medgen/233241" ref="tree=MeSH" title="MedGen record for Non-Neoplastic Retinal Disorder">Non-Neoplastic Retinal Disorder</a></span></li><li><span class="TLline"><a href="/medgen/277432" ref="tree=MeSH" title="MedGen record for Non-Neoplastic Uveal Disorder">Non-Neoplastic Uveal Disorder</a></span></li><li><span class="TLline"><a href="/medgen/507939" ref="tree=MeSH" title="MedGen record for Ocular melanocytosis">Ocular melanocytosis</a></span></li><li><span class="TLline"><a href="/medgen/182689" ref="tree=MeSH" title="MedGen record for Ocular vascular disorder">Ocular vascular disorder</a></span></li><li><span class="TLline"><a href="/medgen/18180" ref="tree=MeSH" title="MedGen record for Optic atrophy">Optic atrophy</a></span></li><li><span class="TLline"><a href="/medgen/6695" ref="tree=MeSH" title="MedGen record for Ornithine aminotransferase deficiency">Ornithine aminotransferase deficiency</a></span></li><li><span class="TLline"><a href="/medgen/14623" ref="tree=MeSH" title="MedGen record for Pars planitis">Pars planitis</a></span></li><li><span class="TLline"><a href="/medgen/313739" ref="tree=MeSH" title="MedGen record for Sunset Syndrome">Sunset Syndrome</a></span></li><li><span class="TLline"><a href="/medgen/226870" ref="tree=MeSH" title="MedGen record for Uveitis-glaucoma-hyphema syndrome">Uveitis-glaucoma-hyphema syndrome</a></span></li><li><span class="TLline"><a href="/medgen/21884" ref="tree=MeSH" title="MedGen record for Vitreous detachment">Vitreous detachment</a></span></li></ul></li><li><span class="TLline"><a href="/medgen/1659001" ref="tree=MeSH" title="MedGen record for Non-Neoplastic Genitourinary System Disorder">Non-Neoplastic Genitourinary System Disorder</a></span><ul><li><span class="TLline"><a href="/medgen/1674313" ref="tree=MeSH" title="MedGen record for Genitourinary syndrome of menopause">Genitourinary syndrome of menopause</a></span></li><li><span class="TLline"><a href="/medgen/266174" ref="tree=MeSH" title="MedGen record for Infectious disease of genitourinary system">Infectious disease of genitourinary system</a></span></li><li><span class="TLline"><a href="/medgen/233781" ref="tree=MeSH" title="MedGen record for Non-Neoplastic Reproductive System Disorder">Non-Neoplastic Reproductive System Disorder</a></span></li><li><span class="TLline"><a href="/medgen/233246" ref="tree=MeSH" title="MedGen record for Non-Neoplastic Urinary System Disorder">Non-Neoplastic Urinary System Disorder</a></span></li></ul></li><li><span class="TLline"><a href="/medgen/233235" ref="tree=MeSH" title="MedGen record for Non-Neoplastic Head and Neck Disorder">Non-Neoplastic Head and Neck Disorder</a></span><ul><li><span class="TLline"><a href="/medgen/3043" ref="tree=MeSH" title="MedGen record for Cholesteatoma">Cholesteatoma</a></span></li><li><span class="TLline"><a href="/medgen/1714608" ref="tree=MeSH" title="MedGen record for Lymphedema of the Head and Neck">Lymphedema of the Head and Neck</a></span></li><li><span class="TLline"><a href="/medgen/233770" ref="tree=MeSH" title="MedGen record for Non-Neoplastic Ear Disorder">Non-Neoplastic Ear Disorder</a></span></li><li><span class="TLline"><a href="/medgen/277427" ref="tree=MeSH" title="MedGen record for Non-Neoplastic Neck Disorder">Non-Neoplastic Neck Disorder</a></span></li><li><span class="TLline"><a href="/medgen/235385" ref="tree=MeSH" title="MedGen record for Non-Neoplastic Oral Disorder">Non-Neoplastic Oral Disorder</a></span></li><li><span class="TLline"><a href="/medgen/277430" ref="tree=MeSH" title="MedGen record for Non-Neoplastic Salivary Gland Disorder">Non-Neoplastic Salivary Gland Disorder</a></span></li><li><span class="TLline"><a href="/medgen/233239" ref="tree=MeSH" title="MedGen record for Non-Neoplastic Sinonasal Disorder">Non-Neoplastic Sinonasal Disorder</a></span></li></ul></li><li><span class="TLline"><a href="/medgen/276575" ref="tree=MeSH" title="MedGen record for Non-Neoplastic Hematopoietic and Lymphoid Cell Disorder">Non-Neoplastic Hematopoietic and Lymphoid Cell Disorder</a></span><ul><li><span class="TLline"><a href="/medgen/604" ref="tree=MeSH" title="MedGen record for Abnormality of the coagulation cascade">Abnormality of the coagulation cascade</a></span></li><li><span class="TLline"><a href="/medgen/362704" ref="tree=MeSH" title="MedGen record for Amegakaryocytosis">Amegakaryocytosis</a></span></li><li><span class="TLline"><a href="/medgen/1526" ref="tree=MeSH" title="MedGen record for Anemia">Anemia</a></span></li><li><span class="TLline"><a href="/medgen/196657" ref="tree=MeSH" title="MedGen record for Benign Lymphoproliferative Disorder">Benign Lymphoproliferative Disorder</a></span></li><li><span class="TLline"><a href="/medgen/760584" ref="tree=MeSH" title="MedGen record for Congenital hematological disorder">Congenital hematological disorder</a></span></li><li><span class="TLline"><a href="/medgen/65121" ref="tree=MeSH" title="MedGen record for Cyclical neutropenia">Cyclical neutropenia</a></span></li><li><span class="TLline"><a href="/medgen/75773" ref="tree=MeSH" title="MedGen record for Evans syndrome">Evans syndrome</a></span></li><li><span class="TLline"><a href="/medgen/507745" ref="tree=MeSH" title="MedGen record for Functional disorder of polymorphonuclear neutrophil">Functional disorder of polymorphonuclear neutrophil</a></span></li><li><span class="TLline"><a href="/medgen/610" ref="tree=MeSH" title="MedGen record for Inherited bleeding disorder, platelet-type">Inherited bleeding disorder, platelet-type</a></span></li><li><span class="TLline"><a href="/medgen/6339" ref="tree=MeSH" title="MedGen record for Methemoglobinemia">Methemoglobinemia</a></span></li><li><span class="TLline"><a href="/medgen/181745" ref="tree=MeSH" title="MedGen record for Neonatal Leukopenia">Neonatal Leukopenia</a></span></li><li><span class="TLline"><a href="/medgen/7471" ref="tree=MeSH" title="MedGen record for Paroxysmal nocturnal hemoglobinuria">Paroxysmal nocturnal hemoglobinuria</a></span></li><li><span class="TLline"><a href="/medgen/11154" ref="tree=MeSH" title="MedGen record for Pure red-cell aplasia">Pure red-cell aplasia</a></span></li><li><span class="TLline"><a href="/medgen/9266" ref="tree=MeSH" title="MedGen record for Sinus histiocytosis with massive lymphadenopathy">Sinus histiocytosis with massive lymphadenopathy</a></span></li><li><span class="TLline"><a href="/medgen/154301" ref="tree=MeSH" title="MedGen record for Spherocytosis">Spherocytosis</a></span></li></ul></li><li><span class="TLline"><a href="/medgen/235384" ref="tree=MeSH" title="MedGen record for Non-Neoplastic Nervous System Disorder">Non-Neoplastic Nervous System Disorder</a></span><ul><li><span class="TLline"><a href="/medgen/105425" ref="tree=MeSH" title="MedGen record for Abnormality of the nervous system">Abnormality of the nervous system</a></span></li><li><span class="TLline"><a href="/medgen/155946" ref="tree=MeSH" title="MedGen record for Autoimmune disorder of the nervous system">Autoimmune disorder of the nervous system</a></span></li><li><span class="TLline"><a href="/medgen/4189" ref="tree=MeSH" title="MedGen record for Demyelinating disease">Demyelinating disease</a></span></li><li><span class="TLline"><a href="/medgen/1684765" ref="tree=MeSH" title="MedGen record for Giant axonal neuropathy">Giant axonal neuropathy</a></span></li><li><span class="TLline"><a href="/medgen/108926" ref="tree=MeSH" title="MedGen record for Infectious disease of the nervous system">Infectious disease of the nervous system</a></span></li><li><span class="TLline"><a href="/medgen/6070" ref="tree=MeSH" title="MedGen record for Leukodystrophy">Leukodystrophy</a></span></li><li><span class="TLline"><a href="/medgen/10230" ref="tree=MeSH" title="MedGen record for Myelitis">Myelitis</a></span></li><li><span class="TLline"><a href="/medgen/75501" ref="tree=MeSH" title="MedGen record for Nerve palsy">Nerve palsy</a></span></li><li><span class="TLline"><a href="/medgen/355075" ref="tree=MeSH" title="MedGen record for Neuronal intranuclear inclusion disease">Neuronal intranuclear inclusion disease</a></span></li><li><span class="TLline"><a href="/medgen/233233" ref="tree=MeSH" title="MedGen record for Non-Neoplastic Central Nervous System Disorder">Non-Neoplastic Central Nervous System Disorder</a></span></li><li><span class="TLline"><a href="/medgen/1669193" ref="tree=MeSH" title="MedGen record for Non-Neoplastic Optic Nerve Disorder">Non-Neoplastic Optic Nerve Disorder</a></span></li><li><span class="TLline"><a href="/medgen/233777" ref="tree=MeSH" title="MedGen record for Non-Neoplastic Peripheral Nervous System Disorder">Non-Neoplastic Peripheral Nervous System Disorder</a></span></li><li><span class="TLline"><a href="/medgen/1744475" ref="tree=MeSH" title="MedGen record for Non-Neoplastic Trigeminal Nerve Disorder">Non-Neoplastic Trigeminal Nerve Disorder</a></span></li></ul></li><li><span class="TLline"><a href="/medgen/233779" ref="tree=MeSH" title="MedGen record for Non-Neoplastic Peritoneal and Retroperitoneal Disorder">Non-Neoplastic Peritoneal and Retroperitoneal Disorder</a></span><ul><li><span class="TLline"><a href="/medgen/233778" ref="tree=MeSH" title="MedGen record for Non-Neoplastic Peritoneal Disorder">Non-Neoplastic Peritoneal Disorder</a></span></li><li><span class="TLline"><a href="/medgen/233242" ref="tree=MeSH" title="MedGen record for Non-Neoplastic Retroperitoneal Disorder">Non-Neoplastic Retroperitoneal Disorder</a></span></li></ul></li><li><span class="TLline"><a href="/medgen/1766542" ref="tree=MeSH" title="MedGen record for Non-Neoplastic Respiratory System Disorder">Non-Neoplastic Respiratory System Disorder</a></span><ul><li><span class="TLline"><a href="/medgen/48425" ref="tree=MeSH" title="MedGen record for Congenital malformation of the respiratory system">Congenital malformation of the respiratory system</a></span></li><li><span class="TLline"><a href="/medgen/11871" ref="tree=MeSH" title="MedGen record for Congenital tracheobronchomegaly">Congenital tracheobronchomegaly</a></span></li><li><span class="TLline"><a href="/medgen/473382" ref="tree=MeSH" title="MedGen record for Neonatal respiratory system disorder">Neonatal respiratory system disorder</a></span></li><li><span class="TLline"><a href="/medgen/1776216" ref="tree=MeSH" title="MedGen record for Non-Neoplastic Chronic Respiratory System Disorder">Non-Neoplastic Chronic Respiratory System Disorder</a></span></li><li><span class="TLline"><a href="/medgen/233236" ref="tree=MeSH" title="MedGen record for Non-Neoplastic Lung Disorder">Non-Neoplastic Lung Disorder</a></span></li><li><span class="TLline"><a href="/medgen/233783" ref="tree=MeSH" title="MedGen record for Non-Neoplastic Tracheal Disorder">Non-Neoplastic Tracheal Disorder</a></span></li><li><span class="TLline"><a href="/medgen/578464" ref="tree=MeSH" title="MedGen record for Postprocedural respiratory disorders">Postprocedural respiratory disorders</a></span></li><li><span class="TLline"><a href="/medgen/1640213" ref="tree=MeSH" title="MedGen record for Sleep-Disordered Breathing">Sleep-Disordered Breathing</a></span></li><li><span class="TLline"><a href="/medgen/137939" ref="tree=MeSH" title="MedGen record for Tracheobronchomalacia">Tracheobronchomalacia</a></span></li></ul></li><li><span class="TLline"><a href="/medgen/233243" ref="tree=MeSH" title="MedGen record for Non-Neoplastic Skin Disorder">Non-Neoplastic Skin Disorder</a></span><ul><li><span class="TLline"><a href="/medgen/75589" ref="tree=MeSH" title="MedGen record for Acrokeratosis verruciformis of Hopf">Acrokeratosis verruciformis of Hopf</a></span></li><li><span class="TLline"><a href="/medgen/266204" ref="tree=MeSH" title="MedGen record for Anetoderma">Anetoderma</a></span></li><li><span class="TLline"><a href="/medgen/1708917" ref="tree=MeSH" title="MedGen record for Atypical Vascular Lesion">Atypical Vascular Lesion</a></span></li><li><span class="TLline"><a href="/medgen/56470" ref="tree=MeSH" title="MedGen record for Bacterial infection of skin">Bacterial infection of skin</a></span></li><li><span class="TLline"><a href="/medgen/10620" ref="tree=MeSH" title="MedGen record for Bullous pemphigoid">Bullous pemphigoid</a></span></li><li><span class="TLline"><a href="/medgen/473184" ref="tree=MeSH" title="MedGen record for Chronic bullous dermatosis of childhood">Chronic bullous dermatosis of childhood</a></span></li><li><span class="TLline"><a href="/medgen/1703247" ref="tree=MeSH" title="MedGen record for Chronic Cutaneous Graft Versus Host Disease">Chronic Cutaneous Graft Versus Host Disease</a></span></li><li><span class="TLline"><a href="/medgen/450991" ref="tree=MeSH" title="MedGen record for Cutaneous abscess">Cutaneous abscess</a></span></li><li><span class="TLline"><a href="/medgen/1712213" ref="tree=MeSH" title="MedGen record for Cutaneous Rosai-Dorfman-Destombes Disease">Cutaneous Rosai-Dorfman-Destombes Disease</a></span></li><li><span class="TLline"><a href="/medgen/8206" ref="tree=MeSH" title="MedGen record for Cutis laxa">Cutis laxa</a></span></li><li><span class="TLline"><a href="/medgen/101793" ref="tree=MeSH" title="MedGen record for Dermal atrophy">Dermal atrophy</a></span></li><li><span class="TLline"><a href="/medgen/41832" ref="tree=MeSH" title="MedGen record for Epidermolysis bullosa">Epidermolysis bullosa</a></span></li><li><span class="TLline"><a href="/medgen/4527" ref="tree=MeSH" title="MedGen record for Erythema multiforme">Erythema multiforme</a></span></li><li><span class="TLline"><a href="/medgen/3767" ref="tree=MeSH" title="MedGen record for Erythroderma">Erythroderma</a></span></li><li><span class="TLline"><a href="/medgen/75587" ref="tree=MeSH" title="MedGen record for Erythrokeratodermia variabilis">Erythrokeratodermia variabilis</a></span></li><li><span class="TLline"><a href="/medgen/42092" ref="tree=MeSH" title="MedGen record for Fox-Fordyce disease">Fox-Fordyce disease</a></span></li><li><span class="TLline"><a href="/medgen/1718790" ref="tree=MeSH" title="MedGen record for Generalized Cutaneous Reticulohistiocytosis">Generalized Cutaneous Reticulohistiocytosis</a></span></li><li><span class="TLline"><a href="/medgen/88319" ref="tree=MeSH" title="MedGen record for Granuloma annulare">Granuloma annulare</a></span></li><li><span class="TLline"><a href="/medgen/224909" ref="tree=MeSH" title="MedGen record for Hamartoma of skin appendage">Hamartoma of skin appendage</a></span></li><li><span class="TLline"><a href="/medgen/1132" ref="tree=MeSH" title="MedGen record for Heloma">Heloma</a></span></li><li><span class="TLline"><a href="/medgen/7002" ref="tree=MeSH" title="MedGen record for Ichthyosis">Ichthyosis</a></span></li><li><span class="TLline"><a href="/medgen/5955" ref="tree=MeSH" title="MedGen record for Keratoderma">Keratoderma</a></span></li><li><span class="TLline"><a href="/medgen/82664" ref="tree=MeSH" title="MedGen record for Keratosis pilaris">Keratosis pilaris</a></span></li><li><span class="TLline"><a href="/medgen/7301" ref="tree=MeSH" title="MedGen record for Lentigo">Lentigo</a></span></li><li><span class="TLline"><a href="/medgen/81385" ref="tree=MeSH" title="MedGen record for Lymphocytoma cutis">Lymphocytoma cutis</a></span></li><li><span class="TLline"><a href="/medgen/45021" ref="tree=MeSH" title="MedGen record for Necrobiosis lipoidica">Necrobiosis lipoidica</a></span></li><li><span class="TLline"><a href="/medgen/537820" ref="tree=MeSH" title="MedGen record for Neonatal toxic erythema">Neonatal toxic erythema</a></span></li><li><span class="TLline"><a href="/medgen/233234" ref="tree=MeSH" title="MedGen record for Non-Neoplastic Hair Disorder">Non-Neoplastic Hair Disorder</a></span></li><li><span class="TLline"><a href="/medgen/78119" ref="tree=MeSH" title="MedGen record for Non-neoplastic nevus">Non-neoplastic nevus</a></span></li><li><span class="TLline"><a href="/medgen/337964" ref="tree=MeSH" title="MedGen record for Parana hard-skin syndrome">Parana hard-skin syndrome</a></span></li><li><span class="TLline"><a href="/medgen/45369" ref="tree=MeSH" title="MedGen record for Pemphigus">Pemphigus</a></span></li><li><span class="TLline"><a href="/medgen/102482" ref="tree=MeSH" title="MedGen record for Pityriasis lichenoides">Pityriasis lichenoides</a></span></li><li><span class="TLline"><a href="/medgen/45939" ref="tree=MeSH" title="MedGen record for Pityriasis rubra pilaris">Pityriasis rubra pilaris</a></span></li><li><span class="TLline"><a href="/medgen/11826" ref="tree=MeSH" title="MedGen record for Pityriasis versicolor">Pityriasis versicolor</a></span></li><li><span class="TLline"><a href="/medgen/97905" ref="tree=MeSH" title="MedGen record for Poikiloderma">Poikiloderma</a></span></li><li><span class="TLline"><a href="/medgen/19534" ref="tree=MeSH" title="MedGen record for Pruritus">Pruritus</a></span></li><li><span class="TLline"><a href="/medgen/235529" ref="tree=MeSH" title="MedGen record for Reactive cutaneous fibrous lesion">Reactive cutaneous fibrous lesion</a></span></li><li><span class="TLline"><a href="/medgen/120476" ref="tree=MeSH" title="MedGen record for Scleromyxedema">Scleromyxedema</a></span></li><li><span class="TLline"><a href="/medgen/20777" ref="tree=MeSH" title="MedGen record for Skin disorder">Skin disorder</a></span></li><li><span class="TLline"><a href="/medgen/57590" ref="tree=MeSH" title="MedGen record for Skin Disorder Arising from Mental Factor">Skin Disorder Arising from Mental Factor</a></span></li><li><span class="TLline"><a href="/medgen/52365" ref="tree=MeSH" title="MedGen record for Skin infection">Skin infection</a></span></li><li><span class="TLline"><a href="/medgen/316465" ref="tree=MeSH" title="MedGen record for Skin pigmentation disorder">Skin pigmentation disorder</a></span></li><li><span class="TLline"><a href="/medgen/19872" ref="tree=MeSH" title="MedGen record for Skin sarcoidosis">Skin sarcoidosis</a></span></li><li><span class="TLline"><a href="/medgen/11452" ref="tree=MeSH" title="MedGen record for Skin tags">Skin tags</a></span></li><li><span class="TLline"><a href="/medgen/48619" ref="tree=MeSH" title="MedGen record for Solar lentigo">Solar lentigo</a></span></li><li><span class="TLline"><a href="/medgen/1708820" ref="tree=MeSH" title="MedGen record for Solitary Cutaneous Reticulohistiocytosis">Solitary Cutaneous Reticulohistiocytosis</a></span></li><li><span class="TLline"><a href="/medgen/52484" ref="tree=MeSH" title="MedGen record for Staphylococcal scalded skin syndrome">Staphylococcal scalded skin syndrome</a></span></li><li><span class="TLline"><a href="/medgen/20955" ref="tree=MeSH" title="MedGen record for Stevens-Johnson syndrome">Stevens-Johnson syndrome</a></span></li><li><span class="TLline"><a href="/medgen/4501" ref="tree=MeSH" title="MedGen record for Toxic epidermal necrolysis">Toxic epidermal necrolysis</a></span></li><li><span class="TLline"><a href="/medgen/91076" ref="tree=MeSH" title="MedGen record for Verruciform xanthoma">Verruciform xanthoma</a></span></li><li><span class="TLline"><a href="/medgen/56357" ref="tree=MeSH" title="MedGen record for Xanthelasma">Xanthelasma</a></span></li><li><span class="TLline"><a href="/medgen/53106" ref="tree=MeSH" title="MedGen record for Xeroderma">Xeroderma</a></span></li></ul></li><li><span class="TLline"><a href="/medgen/233782" ref="tree=MeSH" title="MedGen record for Non-Neoplastic Thoracic Disorder">Non-Neoplastic Thoracic Disorder</a></span><ul><li><span class="TLline"><a href="/medgen/235378" ref="tree=MeSH" title="MedGen record for Non-Neoplastic Axillary Disorder">Non-Neoplastic Axillary Disorder</a></span></li><li><span class="TLline"><a href="/medgen/277423" ref="tree=MeSH" title="MedGen record for Non-Neoplastic Chest Wall Disorder">Non-Neoplastic Chest Wall Disorder</a></span></li><li><span class="TLline"><a href="/medgen/233237" ref="tree=MeSH" title="MedGen record for Non-Neoplastic Mediastinal Disorder">Non-Neoplastic Mediastinal Disorder</a></span></li><li><span class="TLline"><a href="/medgen/235387" ref="tree=MeSH" title="MedGen record for Non-Neoplastic Pleural Disorder">Non-Neoplastic Pleural Disorder</a></span></li><li><span class="TLline"><a href="/medgen/235390" ref="tree=MeSH" title="MedGen record for Non-Neoplastic Thymus Disorder">Non-Neoplastic Thymus Disorder</a></span></li></ul></li><li><span class="TLline"><a href="/medgen/311053" ref="tree=MeSH" title="MedGen record for Non-Neoplastic Vision Disorder">Non-Neoplastic Vision Disorder</a></span><ul><li><span class="TLline"><a href="/medgen/8009" ref="tree=MeSH" title="MedGen record for Amblyopia">Amblyopia</a></span></li><li><span class="TLline"><a href="/medgen/282884" ref="tree=MeSH" title="MedGen record for Ametropia">Ametropia</a></span></li><li><span class="TLline"><a href="/medgen/571" ref="tree=MeSH" title="MedGen record for Binocular vision disease">Binocular vision disease</a></span></li><li><span class="TLline"><a href="/medgen/99138" ref="tree=MeSH" title="MedGen record for Blindness">Blindness</a></span></li><li><span class="TLline"><a href="/medgen/22663" ref="tree=MeSH" title="MedGen record for Reduced vision">Reduced vision</a></span></li><li><span class="TLline"><a href="/medgen/21337" ref="tree=MeSH" title="MedGen record for Strabismus">Strabismus</a></span></li><li><span class="TLline"><a href="/medgen/115959" ref="tree=MeSH" title="MedGen record for Visual agnosia">Visual agnosia</a></span></li></ul></li></ul></li><li><span class="TLline"><a href="/medgen/317955" ref="tree=MeSH" title="MedGen record for Non-Neoplastic Disorder by Special Category">Non-Neoplastic Disorder by Special Category</a></span><ul><li><span class="TLline"><a href="/medgen/90143" ref="tree=MeSH" title="MedGen record for Deformity">Deformity</a></span><ul><li><span class="TLline"><a href="/medgen/310444" ref="tree=MeSH" title="MedGen record for Abnormality of Ventricle">Abnormality of Ventricle</a></span></li><li><span class="TLline"><a href="/medgen/853245" ref="tree=MeSH" title="MedGen record for Cheiromegaly">Cheiromegaly</a></span></li><li><span class="TLline"><a href="/medgen/897815" ref="tree=MeSH" title="MedGen record for Collapsed Lumen">Collapsed Lumen</a></span></li><li><span class="TLline"><a href="/medgen/21767" ref="tree=MeSH" title="MedGen record for Deformity of Forearm">Deformity of Forearm</a></span></li><li><span class="TLline"><a href="/medgen/8359" ref="tree=MeSH" title="MedGen record for Diaphragmatic eventration">Diaphragmatic eventration</a></span></li><li><span class="TLline"><a href="/medgen/310706" ref="tree=MeSH" title="MedGen record for Disfigurement">Disfigurement</a></span></li><li><span class="TLline"><a href="/medgen/4359" ref="tree=MeSH" title="MedGen record for Diverticulum">Diverticulum</a></span></li><li><span class="TLline"><a href="/medgen/903842" ref="tree=MeSH" title="MedGen record for Evagination">Evagination</a></span></li><li><span class="TLline"><a href="/medgen/1254" ref="tree=MeSH" title="MedGen record for Fetal anomaly">Fetal anomaly</a></span></li><li><span class="TLline"><a href="/medgen/5416" ref="tree=MeSH" title="MedGen record for Hallux valgus">Hallux valgus</a></span></li><li><span class="TLline"><a href="/medgen/6816" ref="tree=MeSH" title="MedGen record for Hernia">Hernia</a></span></li><li><span class="TLline"><a href="/medgen/75620" ref="tree=MeSH" title="MedGen record for Heterotaxy">Heterotaxy</a></span></li><li><span class="TLline"><a href="/medgen/44991" ref="tree=MeSH" title="MedGen record for Ingrown nail">Ingrown nail</a></span></li><li><span class="TLline"><a href="/medgen/65141" ref="tree=MeSH" title="MedGen record for Megalencephaly">Megalencephaly</a></span></li><li><span class="TLline"><a href="/medgen/10117" ref="tree=MeSH" title="MedGen record for Mucocele of salivary gland">Mucocele of salivary gland</a></span></li><li><span class="TLline"><a href="/medgen/84298" ref="tree=MeSH" title="MedGen record for Musculoskeletal Deformity">Musculoskeletal Deformity</a></span></li><li><span class="TLline"><a href="/medgen/83332" ref="tree=MeSH" title="MedGen record for Nipple deformity">Nipple deformity</a></span></li><li><span class="TLline"><a href="/medgen/66810" ref="tree=MeSH" title="MedGen record for Nose Deformity">Nose Deformity</a></span></li><li><span class="TLline"><a href="/medgen/42034" ref="tree=MeSH" title="MedGen record for Pes planus">Pes planus</a></span></li><li><span class="TLline"><a href="/medgen/18667" ref="tree=MeSH" title="MedGen record for Prolapse">Prolapse</a></span></li><li><span class="TLline"><a href="/medgen/2287" ref="tree=MeSH" title="MedGen record for Ptosis">Ptosis</a></span></li><li><span class="TLline"><a href="/medgen/5201" ref="tree=MeSH" title="MedGen record for Sinus">Sinus</a></span></li><li><span class="TLline"><a href="/medgen/224710" ref="tree=MeSH" title="MedGen record for Stenosis">Stenosis</a></span></li><li><span class="TLline"><a href="/medgen/83380" ref="tree=MeSH" title="MedGen record for Supernumerary ribs">Supernumerary ribs</a></span></li><li><span class="TLline"><a href="/medgen/1788996" ref="tree=MeSH" title="MedGen record for Tissue or Organ Disruption">Tissue or Organ Disruption</a></span></li></ul></li><li><span class="TLline"><a href="/medgen/224837" ref="tree=MeSH" title="MedGen record for Degenerative disorder">Degenerative disorder</a></span><ul><li><span class="TLline"><a href="/medgen/124363" ref="tree=MeSH" title="MedGen record for Degenerative disease of the central nervous system">Degenerative disease of the central nervous system</a></span></li><li><span class="TLline"><a href="/medgen/233865" ref="tree=MeSH" title="MedGen record for Plexopathy">Plexopathy</a></span></li><li><span class="TLline"><a href="/medgen/236838" ref="tree=MeSH" title="MedGen record for Spinal Degenerative Disorder">Spinal Degenerative Disorder</a></span></li></ul></li><li><span class="TLline"><a href="/medgen/82918" ref="tree=MeSH" title="MedGen record for Endemic disease">Endemic disease</a></span></li><li><span class="TLline"><a href="/medgen/6713" ref="tree=MeSH" title="MedGen record for Hamartoma">Hamartoma</a></span><ul><li><span class="TLline"><a href="/medgen/577255" ref="tree=MeSH" title="MedGen record for Benign Triton Tumor">Benign Triton Tumor</a></span></li><li><span class="TLline"><a href="/medgen/232041" ref="tree=MeSH" title="MedGen record for Central Nervous System Hamartoma">Central Nervous System Hamartoma</a></span></li><li><span class="TLline"><a href="/medgen/313028" ref="tree=MeSH" title="MedGen record for Chondroid hamartoma">Chondroid hamartoma</a></span></li><li><span class="TLline"><a href="/medgen/224911" ref="tree=MeSH" title="MedGen record for Congenital hamartoma">Congenital hamartoma</a></span></li><li><span class="TLline"><a href="/medgen/83107" ref="tree=MeSH" title="MedGen record for Connective tissue nevi">Connective tissue nevi</a></span></li><li><span class="TLline"><a href="/medgen/5420" ref="tree=MeSH" title="MedGen record for Cowden syndrome">Cowden syndrome</a></span></li><li><span class="TLline"><a href="/medgen/724285" ref="tree=MeSH" title="MedGen record for Cutaneous hamartoma">Cutaneous hamartoma</a></span></li><li><span class="TLline"><a href="/medgen/882657" ref="tree=MeSH" title="MedGen record for Cutaneous Neurocristic Hamartoma">Cutaneous Neurocristic Hamartoma</a></span></li><li><span class="TLline"><a href="/medgen/473001" ref="tree=MeSH" title="MedGen record for Ecchordosis physaliphora">Ecchordosis physaliphora</a></span></li><li><span class="TLline"><a href="/medgen/120562" ref="tree=MeSH" title="MedGen record for Fibrous hamartoma">Fibrous hamartoma</a></span></li><li><span class="TLline"><a href="/medgen/313256" ref="tree=MeSH" title="MedGen record for Hamartoma of Mature Cardiac Myocytes">Hamartoma of Mature Cardiac Myocytes</a></span></li><li><span class="TLline"><a href="/medgen/893126" ref="tree=MeSH" title="MedGen record for Hamartoma of the orbital region">Hamartoma of the orbital region</a></span></li><li><span class="TLline"><a href="/medgen/83109" ref="tree=MeSH" title="MedGen record for Hamartomatous polyp">Hamartomatous polyp</a></span></li><li><span class="TLline"><a href="/medgen/474435" ref="tree=MeSH" title="MedGen record for Hamartomatous polyposis">Hamartomatous polyposis</a></span></li><li><span class="TLline"><a href="/medgen/75526" ref="tree=MeSH" title="MedGen record for Hyperpigmentation, progressive cribriform and zosteriform">Hyperpigmentation, progressive cribriform and zosteriform</a></span></li><li><span class="TLline"><a href="/medgen/1646345" ref="tree=MeSH" title="MedGen record for Linear nevus sebaceous syndrome">Linear nevus sebaceous syndrome</a></span></li><li><span class="TLline"><a href="/medgen/609054" ref="tree=MeSH" title="MedGen record for Liver hamartoma">Liver hamartoma</a></span></li><li><span class="TLline"><a href="/medgen/887343" ref="tree=MeSH" title="MedGen record for Meningothelial Hamartoma">Meningothelial Hamartoma</a></span></li><li><span class="TLline"><a href="/medgen/83108" ref="tree=MeSH" title="MedGen record for Mesenchymal hamartoma">Mesenchymal hamartoma</a></span></li><li><span class="TLline"><a href="/medgen/1864173" ref="tree=MeSH" title="MedGen record for Nasal hamartoma">Nasal hamartoma</a></span></li><li><span class="TLline"><a href="/medgen/45181" ref="tree=MeSH" title="MedGen record for Odontoma">Odontoma</a></span></li><li><span class="TLline"><a href="/medgen/120514" ref="tree=MeSH" title="MedGen record for Pallister-Hall syndrome">Pallister-Hall syndrome</a></span></li><li><span class="TLline"><a href="/medgen/1841921" ref="tree=MeSH" title="MedGen record for Pancreatic hamartoma">Pancreatic hamartoma</a></span></li><li><span class="TLline"><a href="/medgen/690113" ref="tree=MeSH" title="MedGen record for Renal hamartoma">Renal hamartoma</a></span></li><li><span class="TLline"><a href="/medgen/354977" ref="tree=MeSH" title="MedGen record for Retinal hamartoma">Retinal hamartoma</a></span></li><li><span class="TLline"><a href="/medgen/1744899" ref="tree=MeSH" title="MedGen record for Sinonasal Respiratory Epithelial Adenomatoid Hamartoma">Sinonasal Respiratory Epithelial Adenomatoid Hamartoma</a></span></li><li><span class="TLline"><a href="/medgen/1736218" ref="tree=MeSH" title="MedGen record for Sinonasal Seromucinous Hamartoma">Sinonasal Seromucinous Hamartoma</a></span></li><li><span class="TLline"><a href="/medgen/699195" ref="tree=MeSH" title="MedGen record for Spleen hamartoma">Spleen hamartoma</a></span></li><li><span class="TLline"><a href="/medgen/22518" ref="tree=MeSH" title="MedGen record for Tuberous sclerosis syndrome">Tuberous sclerosis syndrome</a></span></li><li><span class="TLline"><a href="/medgen/1841625" ref="tree=MeSH" title="MedGen record for Urinary bladder hamartoma">Urinary bladder hamartoma</a></span></li><li><span class="TLline"><a href="/medgen/1782263" ref="tree=MeSH" title="MedGen record for Vascular hamartoma">Vascular hamartoma</a></span></li></ul></li><li><span class="TLline"><a href="/medgen/43784" ref="tree=MeSH" title="MedGen record for Hyperplasia">Hyperplasia</a></span><ul><li><span class="TLline"><a href="/medgen/577383" ref="tree=MeSH" title="MedGen record for Adenomatous Hyperplasia of the Ciliary Body">Adenomatous Hyperplasia of the Ciliary Body</a></span></li><li><span class="TLline"><a href="/medgen/301220" ref="tree=MeSH" title="MedGen record for Adrenal hyperplasia">Adrenal hyperplasia</a></span></li><li><span class="TLline"><a href="/medgen/90732" ref="tree=MeSH" title="MedGen record for Atypical hyperplasia">Atypical hyperplasia</a></span></li><li><span class="TLline"><a href="/medgen/83097" ref="tree=MeSH" title="MedGen record for Basal cell hyperplasia">Basal cell hyperplasia</a></span></li><li><span class="TLline"><a href="/medgen/312369" ref="tree=MeSH" title="MedGen record for Benign prostatic hyperplasia">Benign prostatic hyperplasia</a></span></li><li><span class="TLline"><a href="/medgen/2700" ref="tree=MeSH" title="MedGen record for Bone marrow hyperplasia">Bone marrow hyperplasia</a></span></li><li><span class="TLline"><a href="/medgen/107756" ref="tree=MeSH" title="MedGen record for Breast Hyperplasia">Breast Hyperplasia</a></span></li><li><span class="TLline"><a href="/medgen/927345" ref="tree=MeSH" title="MedGen record for Cervical Mesonephric Remnants and Hyperplasia">Cervical Mesonephric Remnants and Hyperplasia</a></span></li><li><span class="TLline"><a href="/medgen/474359" ref="tree=MeSH" title="MedGen record for Circumferential Endothelial Hyperplasia">Circumferential Endothelial Hyperplasia</a></span></li><li><span class="TLline"><a href="/medgen/1768392" ref="tree=MeSH" title="MedGen record for Conjunctival Reactive Epithelial Hyperplasia">Conjunctival Reactive Epithelial Hyperplasia</a></span></li><li><span class="TLline"><a href="/medgen/473365" ref="tree=MeSH" title="MedGen record for Diffuse hyperplasia">Diffuse hyperplasia</a></span></li><li><span class="TLline"><a href="/medgen/473100" ref="tree=MeSH" title="MedGen record for Drug-induced gingival hyperplasia">Drug-induced gingival hyperplasia</a></span></li><li><span class="TLline"><a href="/medgen/538024" ref="tree=MeSH" title="MedGen record for Epithelial hyperplasia of skin">Epithelial hyperplasia of skin</a></span></li><li><span class="TLline"><a href="/medgen/60066" ref="tree=MeSH" title="MedGen record for Focal epithelial hyperplasia">Focal epithelial hyperplasia</a></span></li><li><span class="TLline"><a href="/medgen/232192" ref="tree=MeSH" title="MedGen record for Foveolar hyperplasia">Foveolar hyperplasia</a></span></li><li><span class="TLline"><a href="/medgen/137710" ref="tree=MeSH" title="MedGen record for Glandular hyperplasia">Glandular hyperplasia</a></span></li><li><span class="TLline"><a href="/medgen/1722651" ref="tree=MeSH" title="MedGen record for Intercalated Duct Hyperplasia">Intercalated Duct Hyperplasia</a></span></li><li><span class="TLline"><a href="/medgen/137709" ref="tree=MeSH" title="MedGen record for Intraductal hyperplasia">Intraductal hyperplasia</a></span></li><li><span class="TLline"><a href="/medgen/272772" ref="tree=MeSH" title="MedGen record for Intraepithelial Melanocytic Hyperplasia">Intraepithelial Melanocytic Hyperplasia</a></span></li><li><span class="TLline"><a href="/medgen/1682321" ref="tree=MeSH" title="MedGen record for Islet Glucagon Cell Hyperplasia">Islet Glucagon Cell Hyperplasia</a></span></li><li><span class="TLline"><a href="/medgen/90735" ref="tree=MeSH" title="MedGen record for Lymphoid hyperplasia">Lymphoid hyperplasia</a></span></li><li><span class="TLline"><a href="/medgen/235320" ref="tree=MeSH" title="MedGen record for Mesonephric Hyperplasia">Mesonephric Hyperplasia</a></span></li><li><span class="TLline"><a href="/medgen/90734" ref="tree=MeSH" title="MedGen record for Mesothelial hyperplasia">Mesothelial hyperplasia</a></span></li><li><span class="TLline"><a href="/medgen/784287" ref="tree=MeSH" title="MedGen record for Multifocal nodular oncocytic hyperplasia of salivary gland">Multifocal nodular oncocytic hyperplasia of salivary gland</a></span></li><li><span class="TLline"><a href="/medgen/837309" ref="tree=MeSH" title="MedGen record for Neuroendocrine cell hyperplasia of infancy">Neuroendocrine cell hyperplasia of infancy</a></span></li><li><span class="TLline"><a href="/medgen/1792204" ref="tree=MeSH" title="MedGen record for Ovarian Leydig Cell Hyperplasia">Ovarian Leydig Cell Hyperplasia</a></span></li><li><span class="TLline"><a href="/medgen/75767" ref="tree=MeSH" title="MedGen record for Parathyroid hyperplasia">Parathyroid hyperplasia</a></span></li><li><span class="TLline"><a href="/medgen/1666905" ref="tree=MeSH" title="MedGen record for Pituitary Hyperplasia">Pituitary Hyperplasia</a></span></li><li><span class="TLline"><a href="/medgen/1773978" ref="tree=MeSH" title="MedGen record for Reactive Epithelial Hyperplasia of the Ciliary Body">Reactive Epithelial Hyperplasia of the Ciliary Body</a></span></li><li><span class="TLline"><a href="/medgen/1729204" ref="tree=MeSH" title="MedGen record for Reactive Hyperplasia of the Retinal Pigment Epithelium">Reactive Hyperplasia of the Retinal Pigment Epithelium</a></span></li><li><span class="TLline"><a href="/medgen/1717117" ref="tree=MeSH" title="MedGen record for Reserve Cell Hyperplasia">Reserve Cell Hyperplasia</a></span></li><li><span class="TLline"><a href="/medgen/19757" ref="tree=MeSH" title="MedGen record for Reticuloendotheliosis, X-linked">Reticuloendotheliosis, X-linked</a></span></li><li><span class="TLline"><a href="/medgen/98352" ref="tree=MeSH" title="MedGen record for Sebaceous hyperplasia">Sebaceous hyperplasia</a></span></li><li><span class="TLline"><a href="/medgen/234815" ref="tree=MeSH" title="MedGen record for Squamous Hyperplasia">Squamous Hyperplasia</a></span></li><li><span class="TLline"><a href="/medgen/83100" ref="tree=MeSH" title="MedGen record for Stromal hyperplasia">Stromal hyperplasia</a></span></li><li><span class="TLline"><a href="/medgen/90975" ref="tree=MeSH" title="MedGen record for Thyroid C cell hyperplasia">Thyroid C cell hyperplasia</a></span></li><li><span class="TLline"><a href="/medgen/234463" ref="tree=MeSH" title="MedGen record for Urothelial hyperplasia">Urothelial hyperplasia</a></span></li></ul></li><li><span class="TLline"><a href="/medgen/452939" ref="tree=MeSH" title="MedGen record for Inflammatory disease">Inflammatory disease</a></span><ul><li><span class="TLline"><a href="/medgen/887040" ref="tree=MeSH" title="MedGen record for Catheter-Related Inflammation">Catheter-Related Inflammation</a></span></li><li><span class="TLline"><a href="/medgen/1057" ref="tree=MeSH" title="MedGen record for Infectious disease">Infectious disease</a></span></li><li><span class="TLline"><a href="/medgen/43877" ref="tree=MeSH" title="MedGen record for Inflammatory bowel disease">Inflammatory bowel disease</a></span></li><li><span class="TLline"><a href="/medgen/215416" ref="tree=MeSH" title="MedGen record for Inflammatory spondylopathy">Inflammatory spondylopathy</a></span></li><li><span class="TLline"><a href="/medgen/901443" ref="tree=MeSH" title="MedGen record for KSHV inflammatory cytokine syndrome">KSHV inflammatory cytokine syndrome</a></span></li><li><span class="TLline"><a href="/medgen/7480" ref="tree=MeSH" title="MedGen record for Mastoiditis">Mastoiditis</a></span></li><li><span class="TLline"><a href="/medgen/87165" ref="tree=MeSH" title="MedGen record for Mucositis">Mucositis</a></span></li></ul></li><li><span class="TLline"><a href="/medgen/44376" ref="tree=MeSH" title="MedGen record for Metabolic disease">Metabolic disease</a></span><ul><li><span class="TLline"><a href="/medgen/82824" ref="tree=MeSH" title="MedGen record for 5,10-Methylenetetrahydrofolate reductase deficiency">5,10-Methylenetetrahydrofolate reductase deficiency</a></span></li><li><span class="TLline"><a href="/medgen/312393" ref="tree=MeSH" title="MedGen record for Abnormal blood ion concentration">Abnormal blood ion concentration</a></span></li><li><span class="TLline"><a href="/medgen/7851" ref="tree=MeSH" title="MedGen record for Abnormality of acid-base homeostasis">Abnormality of acid-base homeostasis</a></span></li><li><span class="TLline"><a href="/medgen/5492" ref="tree=MeSH" title="MedGen record for Bronze diabetes">Bronze diabetes</a></span></li><li><span class="TLline"><a href="/medgen/472889" ref="tree=MeSH" title="MedGen record for Carbohydrate metabolism disease">Carbohydrate metabolism disease</a></span></li><li><span class="TLline"><a href="/medgen/501203" ref="tree=MeSH" title="MedGen record for Carnosinemia">Carnosinemia</a></span></li><li><span class="TLline"><a href="/medgen/1377817" ref="tree=MeSH" title="MedGen record for Combined oxidative phosphorylation defect type 8">Combined oxidative phosphorylation defect type 8</a></span></li><li><span class="TLline"><a href="/medgen/1623699" ref="tree=MeSH" title="MedGen record for Combined oxidative phosphorylation deficiency 33">Combined oxidative phosphorylation deficiency 33</a></span></li><li><span class="TLline"><a href="/medgen/409522" ref="tree=MeSH" title="MedGen record for Dihydropyrimidine dehydrogenase deficiency">Dihydropyrimidine dehydrogenase deficiency</a></span></li><li><span class="TLline"><a href="/medgen/714" ref="tree=MeSH" title="MedGen record for disorder of calcium metabolism">disorder of calcium metabolism</a></span></li><li><span class="TLline"><a href="/medgen/883839" ref="tree=MeSH" title="MedGen record for Disturbance of Temperature Regulation">Disturbance of Temperature Regulation</a></span></li><li><span class="TLline"><a href="/medgen/327583" ref="tree=MeSH" title="MedGen record for DNA Repair-Deficiency Disorders">DNA Repair-Deficiency Disorders</a></span></li><li><span class="TLline"><a href="/medgen/8585" ref="tree=MeSH" title="MedGen record for Emaciated">Emaciated</a></span></li><li><span class="TLline"><a href="/medgen/42280" ref="tree=MeSH" title="MedGen record for Gout">Gout</a></span></li><li><span class="TLline"><a href="/medgen/75700" ref="tree=MeSH" title="MedGen record for Hepatic methionine adenosyltransferase deficiency">Hepatic methionine adenosyltransferase deficiency</a></span></li><li><span class="TLline"><a href="/medgen/322999" ref="tree=MeSH" title="MedGen record for Hepatoencephalopathy due to combined oxidative phosphorylation defect type 1">Hepatoencephalopathy due to combined oxidative phosphorylation defect type 1</a></span></li><li><span class="TLline"><a href="/medgen/343969" ref="tree=MeSH" title="MedGen record for HIGH DENSITY LIPOPROTEIN CHOLESTEROL LEVEL QUANTITATIVE TRAIT LOCUS 6">HIGH DENSITY LIPOPROTEIN CHOLESTEROL LEVEL QUANTITATIVE TRAIT LOCUS 6</a></span></li><li><span class="TLline"><a href="/medgen/162857" ref="tree=MeSH" title="MedGen record for Hyperlactatemia">Hyperlactatemia</a></span></li><li><span class="TLline"><a href="/medgen/9363" ref="tree=MeSH" title="MedGen record for Hyperlipoproteinemia">Hyperlipoproteinemia</a></span></li><li><span class="TLline"><a href="/medgen/82816" ref="tree=MeSH" title="MedGen record for Hyperlysinemia">Hyperlysinemia</a></span></li><li><span class="TLline"><a href="/medgen/79469" ref="tree=MeSH" title="MedGen record for Hyperpipecolatemia">Hyperpipecolatemia</a></span></li><li><span class="TLline"><a href="/medgen/96877" ref="tree=MeSH" title="MedGen record for Hypoalphalipoproteinemia">Hypoalphalipoproteinemia</a></span></li><li><span class="TLline"><a href="/medgen/43799" ref="tree=MeSH" title="MedGen record for Hypophosphatasia">Hypophosphatasia</a></span></li><li><span class="TLline"><a href="/medgen/12140" ref="tree=MeSH" title="MedGen record for Imbalances, Water-Electrolyte">Imbalances, Water-Electrolyte</a></span></li><li><span class="TLline"><a href="/medgen/6323" ref="tree=MeSH" title="MedGen record for Inborn errors of metabolism">Inborn errors of metabolism</a></span></li><li><span class="TLline"><a href="/medgen/57587" ref="tree=MeSH" title="MedGen record for Inherited lipid metabolism disorder">Inherited lipid metabolism disorder</a></span></li><li><span class="TLline"><a href="/medgen/8438" ref="tree=MeSH" title="MedGen record for Iron metabolism disease">Iron metabolism disease</a></span></li><li><span class="TLline"><a href="/medgen/6111" ref="tree=MeSH" title="MedGen record for Lipodystrophy">Lipodystrophy</a></span></li><li><span class="TLline"><a href="/medgen/44256" ref="tree=MeSH" title="MedGen record for Malabsorption syndrome">Malabsorption syndrome</a></span></li><li><span class="TLline"><a href="/medgen/2699" ref="tree=MeSH" title="MedGen record for Metabolic bone disorder">Metabolic bone disorder</a></span></li><li><span class="TLline"><a href="/medgen/647" ref="tree=MeSH" title="MedGen record for Metabolic encephalopathy">Metabolic encephalopathy</a></span></li><li><span class="TLline"><a href="/medgen/155901" ref="tree=MeSH" title="MedGen record for Mitochondrial disease">Mitochondrial disease</a></span></li><li><span class="TLline"><a href="/medgen/853513" ref="tree=MeSH" title="MedGen record for Mitochondrial Enzyme Deficiency">Mitochondrial Enzyme Deficiency</a></span></li><li><span class="TLline"><a href="/medgen/474994" ref="tree=MeSH" title="MedGen record for Nickel Metabolic Disorder">Nickel Metabolic Disorder</a></span></li><li><span class="TLline"><a href="/medgen/811347" ref="tree=MeSH" title="MedGen record for Nutritional disorder">Nutritional disorder</a></span></li><li><span class="TLline"><a href="/medgen/19276" ref="tree=MeSH" title="MedGen record for Phosphorus metabolism disease">Phosphorus metabolism disease</a></span></li><li><span class="TLline"><a href="/medgen/78565" ref="tree=MeSH" title="MedGen record for polysyndactyly">polysyndactyly</a></span></li><li><span class="TLline"><a href="/medgen/10865" ref="tree=MeSH" title="MedGen record for Porphyrin metabolism disease">Porphyrin metabolism disease</a></span></li><li><span class="TLline"><a href="/medgen/403490" ref="tree=MeSH" title="MedGen record for Proteostasis deficiencies">Proteostasis deficiencies</a></span></li><li><span class="TLline"><a href="/medgen/19992" ref="tree=MeSH" title="MedGen record for Skin Diseases, Metabolic">Skin Diseases, Metabolic</a></span></li><li><span class="TLline"><a href="/medgen/22696" ref="tree=MeSH" title="MedGen record for Wasting disease">Wasting disease</a></span></li><li><span class="TLline"><a href="/medgen/472966" ref="tree=MeSH" title="MedGen record for Zinc deficiency">Zinc deficiency</a></span></li></ul></li><li><span class="TLline"><a href="/medgen/1735899" ref="tree=MeSH" title="MedGen record for Non-Communicable Disorder">Non-Communicable Disorder</a></span></li><li><span class="TLline"><a href="/medgen/318102" ref="tree=MeSH" title="MedGen record for Radiation-Related Non-Neoplastic Disorder">Radiation-Related Non-Neoplastic Disorder</a></span><ul><li><span class="TLline"><a href="/medgen/11103" ref="tree=MeSH" title="MedGen record for Dermatitis caused by radiation">Dermatitis caused by radiation</a></span></li><li><span class="TLline"><a href="/medgen/108213" ref="tree=MeSH" title="MedGen record for Fibrous mediastinitis caused by radiation">Fibrous mediastinitis caused by radiation</a></span></li><li><span class="TLline"><a href="/medgen/97884" ref="tree=MeSH" title="MedGen record for Mucositis following radiation therapy">Mucositis following radiation therapy</a></span></li><li><span class="TLline"><a href="/medgen/233903" ref="tree=MeSH" title="MedGen record for Radiation Anemia">Radiation Anemia</a></span></li><li><span class="TLline"><a href="/medgen/120446" ref="tree=MeSH" title="MedGen record for Radiation enteritis of intestine">Radiation enteritis of intestine</a></span></li><li><span class="TLline"><a href="/medgen/311198" ref="tree=MeSH" title="MedGen record for Radiation Sickness Syndrome">Radiation Sickness Syndrome</a></span></li><li><span class="TLline"><a href="/medgen/698356" ref="tree=MeSH" title="MedGen record for Xerostomia caused by ionizing radiation">Xerostomia caused by ionizing radiation</a></span></li></ul></li><li><span class="TLline"><a href="/medgen/354119" ref="tree=MeSH" title="MedGen record for Rare Non-Neoplastic Disorder">Rare Non-Neoplastic Disorder</a></span><ul><li><span class="TLline"><a href="/medgen/162878" ref="tree=MeSH" title="MedGen record for 11q partial monosomy syndrome">11q partial monosomy syndrome</a></span></li><li><span class="TLline"><a href="/medgen/397359" ref="tree=MeSH" title="MedGen record for 17q21 Microdeletion Syndrome">17q21 Microdeletion Syndrome</a></span></li><li><span class="TLline"><a href="/medgen/397089" ref="tree=MeSH" title="MedGen record for 22q Telomere Deletion Syndrome">22q Telomere Deletion Syndrome</a></span></li><li><span class="TLline"><a href="/medgen/75667" ref="tree=MeSH" title="MedGen record for 3-Oxo-5 alpha-steroid delta 4-dehydrogenase deficiency">3-Oxo-5 alpha-steroid delta 4-dehydrogenase deficiency</a></span></li><li><span class="TLline"><a href="/medgen/1253" ref="tree=MeSH" title="MedGen record for Abetalipoproteinaemia">Abetalipoproteinaemia</a></span></li><li><span class="TLline"><a href="/medgen/75679" ref="tree=MeSH" title="MedGen record for Acatalasia">Acatalasia</a></span></li><li><span class="TLline"><a href="/medgen/272277" ref="tree=MeSH" title="MedGen record for Achard syndrome">Achard syndrome</a></span></li><li><span class="TLline"><a href="/medgen/99176" ref="tree=MeSH" title="MedGen record for Achenbach syndrome">Achenbach syndrome</a></span></li><li><span class="TLline"><a href="/medgen/84" ref="tree=MeSH" title="MedGen record for Achondrogenesis">Achondrogenesis</a></span></li><li><span class="TLline"><a href="/medgen/57751" ref="tree=MeSH" title="MedGen record for Achromatopsia">Achromatopsia</a></span></li><li><span class="TLline"><a href="/medgen/162915" ref="tree=MeSH" title="MedGen record for Acrocallosal syndrome">Acrocallosal syndrome</a></span></li><li><span class="TLline"><a href="/medgen/267602" ref="tree=MeSH" title="MedGen record for Acrocephalosyndactyly">Acrocephalosyndactyly</a></span></li><li><span class="TLline"><a href="/medgen/1301" ref="tree=MeSH" title="MedGen record for Acrodermatitis">Acrodermatitis</a></span></li><li><span class="TLline"><a href="/medgen/1611715" ref="tree=MeSH" title="MedGen record for Acrodysostosis 1">Acrodysostosis 1</a></span></li><li><span class="TLline"><a href="/medgen/1304" ref="tree=MeSH" title="MedGen record for Acromegaly">Acromegaly</a></span></li><li><span class="TLline"><a href="/medgen/1790808" ref="tree=MeSH" title="MedGen record for Acromesomelic Dysplasia, PRKG2 Type">Acromesomelic Dysplasia, PRKG2 Type</a></span></li><li><span class="TLline"><a href="/medgen/43097" ref="tree=MeSH" title="MedGen record for Acute febrile neutrophilic dermatosis">Acute febrile neutrophilic dermatosis</a></span></li><li><span class="TLline"><a href="/medgen/56452" ref="tree=MeSH" title="MedGen record for Acute intermittent porphyria">Acute intermittent porphyria</a></span></li><li><span class="TLline"><a href="/medgen/376636" ref="tree=MeSH" title="MedGen record for Acyl-CoA oxidase deficiency">Acyl-CoA oxidase deficiency</a></span></li><li><span class="TLline"><a href="/medgen/82772" ref="tree=MeSH" title="MedGen record for Adenine phosphoribosyltransferase deficiency">Adenine phosphoribosyltransferase deficiency</a></span></li><li><span class="TLline"><a href="/medgen/862975" ref="tree=MeSH" title="MedGen record for ADNP-related multiple congenital anomalies - intellectual disability - autism spectrum disorder">ADNP-related multiple congenital anomalies - intellectual disability - autism spectrum disorder</a></span></li><li><span class="TLline"><a href="/medgen/174" ref="tree=MeSH" title="MedGen record for Agnosia">Agnosia</a></span></li><li><span class="TLline"><a href="/medgen/61236" ref="tree=MeSH" title="MedGen record for Aicardi syndrome">Aicardi syndrome</a></span></li><li><span class="TLline"><a href="/medgen/1381" ref="tree=MeSH" title="MedGen record for Ainhum">Ainhum</a></span></li><li><span class="TLline"><a href="/medgen/182" ref="tree=MeSH" title="MedGen record for Albinism">Albinism</a></span></li><li><span class="TLline"><a href="/medgen/1413" ref="tree=MeSH" title="MedGen record for Alkaptonuria">Alkaptonuria</a></span></li><li><span class="TLline"><a href="/medgen/208645" ref="tree=MeSH" title="MedGen record for Allan-Herndon-Dudley syndrome">Allan-Herndon-Dudley syndrome</a></span></li><li><span class="TLline"><a href="/medgen/337145" ref="tree=MeSH" title="MedGen record for Alpha thalassemia-X-linked intellectual disability syndrome">Alpha thalassemia-X-linked intellectual disability syndrome</a></span></li><li><span class="TLline"><a href="/medgen/482058" ref="tree=MeSH" title="MedGen record for Alpha-methylacyl-CoA racemase deficiency">Alpha-methylacyl-CoA racemase deficiency</a></span></li><li><span class="TLline"><a href="/medgen/78675" ref="tree=MeSH" title="MedGen record for Alstrom syndrome">Alstrom syndrome</a></span></li><li><span class="TLline"><a href="/medgen/164210" ref="tree=MeSH" title="MedGen record for Analbuminemia">Analbuminemia</a></span></li><li><span class="TLline"><a href="/medgen/98312" ref="tree=MeSH" title="MedGen record for Anaphylotoxin inactivator deficiency">Anaphylotoxin inactivator deficiency</a></span></li><li><span class="TLline"><a href="/medgen/327586" ref="tree=MeSH" title="MedGen record for Andersen Tawil syndrome">Andersen Tawil syndrome</a></span></li><li><span class="TLline"><a href="/medgen/8068" ref="tree=MeSH" title="MedGen record for Anencephaly">Anencephaly</a></span></li><li><span class="TLline"><a href="/medgen/9646" ref="tree=MeSH" title="MedGen record for Angioosteohypertrophic syndrome">Angioosteohypertrophic syndrome</a></span></li><li><span class="TLline"><a href="/medgen/98032" ref="tree=MeSH" title="MedGen record for Ankyloblepharon-ectodermal defects-cleft lip/palate syndrome">Ankyloblepharon-ectodermal defects-cleft lip/palate syndrome</a></span></li><li><span class="TLline"><a href="/medgen/140788" ref="tree=MeSH" title="MedGen record for Anti-glomerular basement membrane disease">Anti-glomerular basement membrane disease</a></span></li><li><span class="TLline"><a href="/medgen/461449" ref="tree=MeSH" title="MedGen record for Antley-Bixler syndrome with genital anomalies and disordered steroidogenesis">Antley-Bixler syndrome with genital anomalies and disordered steroidogenesis</a></span></li><li><span class="TLline"><a href="/medgen/140908" ref="tree=MeSH" title="MedGen record for Aprosencephaly">Aprosencephaly</a></span></li><li><span class="TLline"><a href="/medgen/78688" ref="tree=MeSH" title="MedGen record for Arginase deficiency">Arginase deficiency</a></span></li><li><span class="TLline"><a href="/medgen/78687" ref="tree=MeSH" title="MedGen record for Argininosuccinate lyase deficiency">Argininosuccinate lyase deficiency</a></span></li><li><span class="TLline"><a href="/medgen/87618" ref="tree=MeSH" title="MedGen record for Arrhythmogenic right ventricular cardiomyopathy">Arrhythmogenic right ventricular cardiomyopathy</a></span></li><li><span class="TLline"><a href="/medgen/1631685" ref="tree=MeSH" title="MedGen record for Arterial calcification, generalized, of infancy, 1">Arterial calcification, generalized, of infancy, 1</a></span></li><li><span class="TLline"><a href="/medgen/2455" ref="tree=MeSH" title="MedGen record for Arthrogryposis">Arthrogryposis</a></span></li><li><span class="TLline"><a href="/medgen/861227" ref="tree=MeSH" title="MedGen record for Ataxia-telangiectasia-like disorder 1">Ataxia-telangiectasia-like disorder 1</a></span></li><li><span class="TLline"><a href="/medgen/105489" ref="tree=MeSH" title="MedGen record for Atransferrinemia">Atransferrinemia</a></span></li><li><span class="TLline"><a href="/medgen/75615" ref="tree=MeSH" title="MedGen record for Atrophia bulborum hereditaria">Atrophia bulborum hereditaria</a></span></li><li><span class="TLline"><a href="/medgen/156267" ref="tree=MeSH" title="MedGen record for Atrophic muscular disease">Atrophic muscular disease</a></span></li><li><span class="TLline"><a href="/medgen/2129" ref="tree=MeSH" title="MedGen record for Auditory processing disorder">Auditory processing disorder</a></span></li><li><span class="TLline"><a href="/medgen/382676" ref="tree=MeSH" title="MedGen record for Autosomal dominant deafness - onychodystrophy syndrome">Autosomal dominant deafness - onychodystrophy syndrome</a></span></li><li><span class="TLline"><a href="/medgen/325000" ref="tree=MeSH" title="MedGen record for Autosomal dominant polycystic kidney disease type 1 with tuberous sclerosis">Autosomal dominant polycystic kidney disease type 1 with tuberous sclerosis</a></span></li><li><span class="TLline"><a href="/medgen/382128" ref="tree=MeSH" title="MedGen record for Autosomal recessive DOPA responsive dystonia">Autosomal recessive DOPA responsive dystonia</a></span></li><li><span class="TLline"><a href="/medgen/96067" ref="tree=MeSH" title="MedGen record for Autosomal recessive hypohidrotic ectodermal dysplasia syndrome">Autosomal recessive hypohidrotic ectodermal dysplasia syndrome</a></span></li><li><span class="TLline"><a href="/medgen/761234" ref="tree=MeSH" title="MedGen record for Autosomal recessive nonsyndromic hearing loss 4">Autosomal recessive nonsyndromic hearing loss 4</a></span></li><li><span class="TLline"><a href="/medgen/342839" ref="tree=MeSH" title="MedGen record for Autosomal recessive nonsyndromic hearing loss 28">Autosomal recessive nonsyndromic hearing loss 28</a></span></li><li><span class="TLline"><a href="/medgen/374909" ref="tree=MeSH" title="MedGen record for Autosomal recessive nonsyndromic hearing loss 39">Autosomal recessive nonsyndromic hearing loss 39</a></span></li><li><span class="TLline"><a href="/medgen/346670" ref="tree=MeSH" title="MedGen record for Autosomal recessive nonsyndromic hearing loss 49">Autosomal recessive nonsyndromic hearing loss 49</a></span></li><li><span class="TLline"><a href="/medgen/811487" ref="tree=MeSH" title="MedGen record for Axenfeld-Rieger syndrome type 1">Axenfeld-Rieger syndrome type 1</a></span></li><li><span class="TLline"><a href="/medgen/9841" ref="tree=MeSH" title="MedGen record for Azorean disease">Azorean disease</a></span></li><li><span class="TLline"><a href="/medgen/2172" ref="tree=MeSH" title="MedGen record for Bartter syndrome">Bartter syndrome</a></span></li><li><span class="TLline"><a href="/medgen/108185" ref="tree=MeSH" title="MedGen record for Beaded hair">Beaded hair</a></span></li><li><span class="TLline"><a href="/medgen/377668" ref="tree=MeSH" title="MedGen record for Beare-Stevenson cutis gyrata syndrome">Beare-Stevenson cutis gyrata syndrome</a></span></li><li><span class="TLline"><a href="/medgen/18732" ref="tree=MeSH" title="MedGen record for Benign intracranial hypertension">Benign intracranial hypertension</a></span></li><li><span class="TLline"><a href="/medgen/10619" ref="tree=MeSH" title="MedGen record for Benign mucous membrane pemphigoid">Benign mucous membrane pemphigoid</a></span></li><li><span class="TLline"><a href="/medgen/2212" ref="tree=MeSH" title="MedGen record for Bernard Soulier syndrome">Bernard Soulier syndrome</a></span></li><li><span class="TLline"><a href="/medgen/417702" ref="tree=MeSH" title="MedGen record for Beta-Methylcrotonylglycinuria">Beta-Methylcrotonylglycinuria</a></span></li><li><span class="TLline"><a href="/medgen/137982" ref="tree=MeSH" title="MedGen record for Bifunctional peroxisomal enzyme deficiency">Bifunctional peroxisomal enzyme deficiency</a></span></li><li><span class="TLline"><a href="/medgen/44018" ref="tree=MeSH" title="MedGen record for Bilirubin encephalopathy">Bilirubin encephalopathy</a></span></li><li><span class="TLline"><a href="/medgen/66323" ref="tree=MeSH" title="MedGen record for Biotinidase deficiency">Biotinidase deficiency</a></span></li><li><span class="TLline"><a href="/medgen/78557" ref="tree=MeSH" title="MedGen record for Borjeson-Forssman-Lehmann syndrome">Borjeson-Forssman-Lehmann syndrome</a></span></li><li><span class="TLline"><a href="/medgen/69225" ref="tree=MeSH" title="MedGen record for Brown-Séquard syndrome">Brown-Séquard syndrome</a></span></li><li><span class="TLline"><a href="/medgen/2404" ref="tree=MeSH" title="MedGen record for Calciphylaxis">Calciphylaxis</a></span></li><li><span class="TLline"><a href="/medgen/354620" ref="tree=MeSH" title="MedGen record for Camptomelic dysplasia">Camptomelic dysplasia</a></span></li><li><span class="TLline"><a href="/medgen/10366" ref="tree=MeSH" title="MedGen record for Cancrum oris">Cancrum oris</a></span></li><li><span class="TLline"><a href="/medgen/864369" ref="tree=MeSH" title="MedGen record for Carbonic anhydrase I deficiency">Carbonic anhydrase I deficiency</a></span></li><li><span class="TLline"><a href="/medgen/266149" ref="tree=MeSH" title="MedGen record for Cardio-facio-cutaneous syndrome">Cardio-facio-cutaneous syndrome</a></span></li><li><span class="TLline"><a href="/medgen/91000" ref="tree=MeSH" title="MedGen record for Carnitine acylcarnitine translocase deficiency">Carnitine acylcarnitine translocase deficiency</a></span></li><li><span class="TLline"><a href="/medgen/316820" ref="tree=MeSH" title="MedGen record for Carnitine palmitoyl transferase 1A deficiency">Carnitine palmitoyl transferase 1A deficiency</a></span></li><li><span class="TLline"><a href="/medgen/137978" ref="tree=MeSH" title="MedGen record for Carnitine palmitoyltransferase II deficiency">Carnitine palmitoyltransferase II deficiency</a></span></li><li><span class="TLline"><a href="/medgen/57924" ref="tree=MeSH" title="MedGen record for Caroli disease">Caroli disease</a></span></li><li><span class="TLline"><a href="/medgen/120543" ref="tree=MeSH" title="MedGen record for Cat eye syndrome">Cat eye syndrome</a></span></li><li><span class="TLline"><a href="/medgen/2862" ref="tree=MeSH" title="MedGen record for Cataplexy">Cataplexy</a></span></li><li><span class="TLline"><a href="/medgen/199687" ref="tree=MeSH" title="MedGen record for Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy">Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy</a></span></li><li><span class="TLline"><a href="/medgen/137896" ref="tree=MeSH" title="MedGen record for Cerebral cysticercosis">Cerebral cysticercosis</a></span></li><li><span class="TLline"><a href="/medgen/344563" ref="tree=MeSH" title="MedGen record for Channelopathy-associated congenital insensitivity to pain, autosomal recessive">Channelopathy-associated congenital insensitivity to pain, autosomal recessive</a></span></li><li><span class="TLline"><a href="/medgen/75567" ref="tree=MeSH" title="MedGen record for CHARGE syndrome">CHARGE syndrome</a></span></li><li><span class="TLline"><a href="/medgen/2065" ref="tree=MeSH" title="MedGen record for Chiari malformation">Chiari malformation</a></span></li><li><span class="TLline"><a href="/medgen/886" ref="tree=MeSH" title="MedGen record for Chilblains">Chilblains</a></span></li><li><span class="TLline"><a href="/medgen/116041" ref="tree=MeSH" title="MedGen record for Cholestanol storage disease">Cholestanol storage disease</a></span></li><li><span class="TLline"><a href="/medgen/78658" ref="tree=MeSH" title="MedGen record for Cholestasis-edema syndrome, Norwegian type">Cholestasis-edema syndrome, Norwegian type</a></span></li><li><span class="TLline"><a href="/medgen/3052" ref="tree=MeSH" title="MedGen record for Chondrodysplasia punctata">Chondrodysplasia punctata</a></span></li><li><span class="TLline"><a href="/medgen/3420" ref="tree=MeSH" title="MedGen record for Chorea">Chorea</a></span></li><li><span class="TLline"><a href="/medgen/98277" ref="tree=MeSH" title="MedGen record for Chorea-acanthocytosis">Chorea-acanthocytosis</a></span></li><li><span class="TLline"><a href="/medgen/334629" ref="tree=MeSH" title="MedGen record for Chromosome 1p36 deletion syndrome">Chromosome 1p36 deletion syndrome</a></span></li><li><span class="TLline"><a href="/medgen/419169" ref="tree=MeSH" title="MedGen record for Chromosome 2q37 deletion syndrome">Chromosome 2q37 deletion syndrome</a></span></li><li><span class="TLline"><a href="/medgen/3486" ref="tree=MeSH" title="MedGen record for Cleidocranial dysostosis">Cleidocranial dysostosis</a></span></li><li><span class="TLline"><a href="/medgen/1617" ref="tree=MeSH" title="MedGen record for Coarctation of aorta">Coarctation of aorta</a></span></li><li><span class="TLline"><a href="/medgen/333031" ref="tree=MeSH" title="MedGen record for CODAS syndrome">CODAS syndrome</a></span></li><li><span class="TLline"><a href="/medgen/334528" ref="tree=MeSH" title="MedGen record for Coenzyme Q10 deficiency">Coenzyme Q10 deficiency</a></span></li><li><span class="TLline"><a href="/medgen/75556" ref="tree=MeSH" title="MedGen record for Coffin-Lowry syndrome">Coffin-Lowry syndrome</a></span></li><li><span class="TLline"><a href="/medgen/1762238" ref="tree=MeSH" title="MedGen record for COFS syndrome">COFS syndrome</a></span></li><li><span class="TLline"><a href="/medgen/218910" ref="tree=MeSH" title="MedGen record for Cogan-Reese syndrome">Cogan-Reese syndrome</a></span></li><li><span class="TLline"><a href="/medgen/75652" ref="tree=MeSH" title="MedGen record for Combined molybdoflavoprotein enzyme deficiency">Combined molybdoflavoprotein enzyme deficiency</a></span></li><li><span class="TLline"><a href="/medgen/11159" ref="tree=MeSH" title="MedGen record for Complex regional pain syndrome type 1">Complex regional pain syndrome type 1</a></span></li><li><span class="TLline"><a href="/medgen/2918" ref="tree=MeSH" title="MedGen record for Complex regional pain syndrome type 2">Complex regional pain syndrome type 2</a></span></li><li><span class="TLline"><a href="/medgen/272171" ref="tree=MeSH" title="MedGen record for Congenital amegakaryocytic thrombocytopenia">Congenital amegakaryocytic thrombocytopenia</a></span></li><li><span class="TLline"><a href="/medgen/1941" ref="tree=MeSH" title="MedGen record for Congenital aniridia">Congenital aniridia</a></span></li><li><span class="TLline"><a href="/medgen/98021" ref="tree=MeSH" title="MedGen record for Congenital bilateral aplasia of vas deferens from CFTR mutation">Congenital bilateral aplasia of vas deferens from CFTR mutation</a></span></li><li><span class="TLline"><a href="/medgen/83348" ref="tree=MeSH" title="MedGen record for Congenital defect of folate absorption">Congenital defect of folate absorption</a></span></li><li><span class="TLline"><a href="/medgen/815321" ref="tree=MeSH" title="MedGen record for Congenital disorder of deglycosylation">Congenital disorder of deglycosylation</a></span></li><li><span class="TLline"><a href="/medgen/76469" ref="tree=MeSH" title="MedGen record for Congenital disorder of glycosylation">Congenital disorder of glycosylation</a></span></li><li><span class="TLline"><a href="/medgen/8064" ref="tree=MeSH" title="MedGen record for Congenital dyserythropoietic anemia">Congenital dyserythropoietic anemia</a></span></li><li><span class="TLline"><a href="/medgen/67438" ref="tree=MeSH" title="MedGen record for Congenital generalized lipodystrophy">Congenital generalized lipodystrophy</a></span></li><li><span class="TLline"><a href="/medgen/816301" ref="tree=MeSH" title="MedGen record for Congenital microcephaly - severe encephalopathy - progressive cerebral atrophy syndrome">Congenital microcephaly - severe encephalopathy - progressive cerebral atrophy syndrome</a></span></li><li><span class="TLline"><a href="/medgen/340597" ref="tree=MeSH" title="MedGen record for Congenital multicore myopathy with external ophthalmoplegia">Congenital multicore myopathy with external ophthalmoplegia</a></span></li><li><span class="TLline"><a href="/medgen/155650" ref="tree=MeSH" title="MedGen record for Congenital myasthenic syndrome">Congenital myasthenic syndrome</a></span></li><li><span class="TLline"><a href="/medgen/108177" ref="tree=MeSH" title="MedGen record for Congenital myopathy with fiber type disproportion">Congenital myopathy with fiber type disproportion</a></span></li><li><span class="TLline"><a href="/medgen/539398" ref="tree=MeSH" title="MedGen record for Congenital pseudoarthrosis of the tibia">Congenital pseudoarthrosis of the tibia</a></span></li><li><span class="TLline"><a href="/medgen/6916" ref="tree=MeSH" title="MedGen record for Congenital sensory neuropathy with selective loss of small myelinated fibers">Congenital sensory neuropathy with selective loss of small myelinated fibers</a></span></li><li><span class="TLline"><a href="/medgen/156050" ref="tree=MeSH" title="MedGen record for Congenital structural myopathy">Congenital structural myopathy</a></span></li><li><span class="TLline"><a href="/medgen/265" ref="tree=MeSH" title="MedGen record for Constriction ring syndrome">Constriction ring syndrome</a></span></li><li><span class="TLline"><a href="/medgen/1639771" ref="tree=MeSH" title="MedGen record for Cortical Dysplasia-Focal Epilepsy Syndrome">Cortical Dysplasia-Focal Epilepsy Syndrome</a></span></li><li><span class="TLline"><a href="/medgen/6035" ref="tree=MeSH" title="MedGen record for Coxa plana">Coxa plana</a></span></li><li><span class="TLline"><a href="/medgen/1641011" ref="tree=MeSH" title="MedGen record for Cranioectodermal dysplasia">Cranioectodermal dysplasia</a></span></li><li><span class="TLline"><a href="/medgen/75554" ref="tree=MeSH" title="MedGen record for Craniofacial microsomia">Craniofacial microsomia</a></span></li><li><span class="TLline"><a href="/medgen/1163" ref="tree=MeSH" title="MedGen record for Craniosynostosis syndrome">Craniosynostosis syndrome</a></span></li><li><span class="TLline"><a href="/medgen/1162" ref="tree=MeSH" title="MedGen record for Crouzon syndrome">Crouzon syndrome</a></span></li><li><span class="TLline"><a href="/medgen/412215" ref="tree=MeSH" title="MedGen record for Cryopyrin associated periodic syndrome">Cryopyrin associated periodic syndrome</a></span></li><li><span class="TLline"><a href="/medgen/82692" ref="tree=MeSH" title="MedGen record for Cryptophthalmos syndrome">Cryptophthalmos syndrome</a></span></li><li><span class="TLline"><a href="/medgen/1693375" ref="tree=MeSH" title="MedGen record for Crystal-Storing Histiocytosis">Crystal-Storing Histiocytosis</a></span></li><li><span class="TLline"><a href="/medgen/66353" ref="tree=MeSH" title="MedGen record for Cystathioninuria">Cystathioninuria</a></span></li><li><span class="TLline"><a href="/medgen/8226" ref="tree=MeSH" title="MedGen record for Cystinuria">Cystinuria</a></span></li><li><span class="TLline"><a href="/medgen/75662" ref="tree=MeSH" title="MedGen record for Cytochrome-c oxidase deficiency">Cytochrome-c oxidase deficiency</a></span></li><li><span class="TLline"><a href="/medgen/452447" ref="tree=MeSH" title="MedGen record for D-Glyceric aciduria">D-Glyceric aciduria</a></span></li><li><span class="TLline"><a href="/medgen/4150" ref="tree=MeSH" title="MedGen record for Dandy-Walker syndrome">Dandy-Walker syndrome</a></span></li><li><span class="TLline"><a href="/medgen/78752" ref="tree=MeSH" title="MedGen record for De Lange syndrome">De Lange syndrome</a></span></li><li><span class="TLline"><a href="/medgen/75550" ref="tree=MeSH" title="MedGen record for DE SANCTIS-CACCHIONE SYNDROME">DE SANCTIS-CACCHIONE SYNDROME</a></span></li><li><span class="TLline"><a href="/medgen/1793876" ref="tree=MeSH" title="MedGen record for Deafness due to Connexin 26 Gene Anomaly">Deafness due to Connexin 26 Gene Anomaly</a></span></li><li><span class="TLline"><a href="/medgen/220945" ref="tree=MeSH" title="MedGen record for Deficiency of aromatic-L-amino-acid decarboxylase">Deficiency of aromatic-L-amino-acid decarboxylase</a></span></li><li><span class="TLline"><a href="/medgen/90998" ref="tree=MeSH" title="MedGen record for Deficiency of butyryl-CoA dehydrogenase">Deficiency of butyryl-CoA dehydrogenase</a></span></li><li><span class="TLline"><a href="/medgen/78692" ref="tree=MeSH" title="MedGen record for Deficiency of hydroxymethylglutaryl-CoA lyase">Deficiency of hydroxymethylglutaryl-CoA lyase</a></span></li><li><span class="TLline"><a href="/medgen/370754" ref="tree=MeSH" title="MedGen record for Deficiency of isobutyryl-CoA dehydrogenase">Deficiency of isobutyryl-CoA dehydrogenase</a></span></li><li><span class="TLline"><a href="/medgen/87453" ref="tree=MeSH" title="MedGen record for Deficiency of mevalonate kinase">Deficiency of mevalonate kinase</a></span></li><li><span class="TLline"><a href="/medgen/96605" ref="tree=MeSH" title="MedGen record for Deletion of long arm of chromosome 18">Deletion of long arm of chromosome 18</a></span></li><li><span class="TLline"><a href="/medgen/96604" ref="tree=MeSH" title="MedGen record for Deletion of short arm of chromosome 18">Deletion of short arm of chromosome 18</a></span></li><li><span class="TLline"><a href="/medgen/155630" ref="tree=MeSH" title="MedGen record for Dentatorubral-pallidoluysian atrophy">Dentatorubral-pallidoluysian atrophy</a></span></li><li><span class="TLline"><a href="/medgen/8313" ref="tree=MeSH" title="MedGen record for Dentinogenesis imperfecta">Dentinogenesis imperfecta</a></span></li><li><span class="TLline"><a href="/medgen/4255" ref="tree=MeSH" title="MedGen record for Dextrocardia">Dextrocardia</a></span></li><li><span class="TLline"><a href="/medgen/4268" ref="tree=MeSH" title="MedGen record for Diaphyseal dysplasia">Diaphyseal dysplasia</a></span></li><li><span class="TLline"><a href="/medgen/113103" ref="tree=MeSH" title="MedGen record for Diastrophic dysplasia">Diastrophic dysplasia</a></span></li><li><span class="TLline"><a href="/medgen/5695" ref="tree=MeSH" title="MedGen record for Diffuse idiopathic skeletal hyperostosis">Diffuse idiopathic skeletal hyperostosis</a></span></li><li><span class="TLline"><a href="/medgen/57634" ref="tree=MeSH" title="MedGen record for Digital flexor tenosynovitis">Digital flexor tenosynovitis</a></span></li><li><span class="TLline"><a href="/medgen/57586" ref="tree=MeSH" title="MedGen record for Disorder of the urea cycle metabolism">Disorder of the urea cycle metabolism</a></span></li><li><span class="TLline"><a href="/medgen/339855" ref="tree=MeSH" title="MedGen record for DNA ligase IV deficiency">DNA ligase IV deficiency</a></span></li><li><span class="TLline"><a href="/medgen/1647918" ref="tree=MeSH" title="MedGen record for Dominant hereditary optic atrophy">Dominant hereditary optic atrophy</a></span></li><li><span class="TLline"><a href="/medgen/473794" ref="tree=MeSH" title="MedGen record for Double Y syndrome">Double Y syndrome</a></span></li><li><span class="TLline"><a href="/medgen/886101" ref="tree=MeSH" title="MedGen record for Drug- and Toxin-Induced Pulmonary Arterial Hypertension">Drug- and Toxin-Induced Pulmonary Arterial Hypertension</a></span></li><li><span class="TLline"><a href="/medgen/4413" ref="tree=MeSH" title="MedGen record for Duane retraction syndrome">Duane retraction syndrome</a></span></li><li><span class="TLline"><a href="/medgen/59797" ref="tree=MeSH" title="MedGen record for Dubowitz syndrome">Dubowitz syndrome</a></span></li><li><span class="TLline"><a href="/medgen/120527" ref="tree=MeSH" title="MedGen record for Dyggve-Melchior-Clausen syndrome">Dyggve-Melchior-Clausen syndrome</a></span></li><li><span class="TLline"><a href="/medgen/4435" ref="tree=MeSH" title="MedGen record for Ebstein anomaly">Ebstein anomaly</a></span></li><li><span class="TLline"><a href="/medgen/375786" ref="tree=MeSH" title="MedGen record for Ectodermal dysplasia and immune deficiency">Ectodermal dysplasia and immune deficiency</a></span></li><li><span class="TLline"><a href="/medgen/78566" ref="tree=MeSH" title="MedGen record for Ectrodactyly">Ectrodactyly</a></span></li><li><span class="TLline"><a href="/medgen/3966" ref="tree=MeSH" title="MedGen record for Ectromelia">Ectromelia</a></span></li><li><span class="TLline"><a href="/medgen/1385012" ref="tree=MeSH" title="MedGen record for Eiken Type Chondrodysplasia">Eiken Type Chondrodysplasia</a></span></li><li><span class="TLline"><a href="/medgen/8584" ref="tree=MeSH" title="MedGen record for Ellis-van Creveld syndrome">Ellis-van Creveld syndrome</a></span></li><li><span class="TLline"><a href="/medgen/41766" ref="tree=MeSH" title="MedGen record for Empty sella syndrome">Empty sella syndrome</a></span></li><li><span class="TLline"><a href="/medgen/1646412" ref="tree=MeSH" title="MedGen record for Encephalocele">Encephalocele</a></span></li><li><span class="TLline"><a href="/medgen/1641798" ref="tree=MeSH" title="MedGen record for Epilepsy, familial focal, with variable foci 1">Epilepsy, familial focal, with variable foci 1</a></span></li><li><span class="TLline"><a href="/medgen/8687" ref="tree=MeSH" title="MedGen record for Erythromelalgia">Erythromelalgia</a></span></li><li><span class="TLline"><a href="/medgen/102408" ref="tree=MeSH" title="MedGen record for Erythropoietic porphyria">Erythropoietic porphyria</a></span></li><li><span class="TLline"><a href="/medgen/56455" ref="tree=MeSH" title="MedGen record for Erythropoietic protoporphyria">Erythropoietic protoporphyria</a></span></li><li><span class="TLline"><a href="/medgen/338020" ref="tree=MeSH" title="MedGen record for Exstrophy-epispadias complex">Exstrophy-epispadias complex</a></span></li><li><span class="TLline"><a href="/medgen/473218" ref="tree=MeSH" title="MedGen record for Factor V Leiden mutation">Factor V Leiden mutation</a></span></li><li><span class="TLline"><a href="/medgen/98464" ref="tree=MeSH" title="MedGen record for Familial aplasia of the vermis">Familial aplasia of the vermis</a></span></li><li><span class="TLline"><a href="/medgen/335678" ref="tree=MeSH" title="MedGen record for Familial digital arthropathy-brachydactyly">Familial digital arthropathy-brachydactyly</a></span></li><li><span class="TLline"><a href="/medgen/41678" ref="tree=MeSH" title="MedGen record for Familial dysautonomia">Familial dysautonomia</a></span></li><li><span class="TLline"><a href="/medgen/816229" ref="tree=MeSH" title="MedGen record for Familial episodic pain syndrome with predominantly lower limb involvement">Familial episodic pain syndrome with predominantly lower limb involvement</a></span></li><li><span class="TLline"><a href="/medgen/75681" ref="tree=MeSH" title="MedGen record for Familial hypokalemia-hypomagnesemia">Familial hypokalemia-hypomagnesemia</a></span></li><li><span class="TLline"><a href="/medgen/45811" ref="tree=MeSH" title="MedGen record for Familial Mediterranean fever">Familial Mediterranean fever</a></span></li><li><span class="TLline"><a href="/medgen/124408" ref="tree=MeSH" title="MedGen record for Familial partial lipodystrophy">Familial partial lipodystrophy</a></span></li><li><span class="TLline"><a href="/medgen/18291" ref="tree=MeSH" title="MedGen record for Familial periodic paralysis">Familial periodic paralysis</a></span></li><li><span class="TLline"><a href="/medgen/78654" ref="tree=MeSH" title="MedGen record for Farber lipogranulomatosis">Farber lipogranulomatosis</a></span></li><li><span class="TLline"><a href="/medgen/104768" ref="tree=MeSH" title="MedGen record for Fatal familial insomnia">Fatal familial insomnia</a></span></li><li><span class="TLline"><a href="/medgen/163209" ref="tree=MeSH" title="MedGen record for Feingold syndrome">Feingold syndrome</a></span></li><li><span class="TLline"><a href="/medgen/4674" ref="tree=MeSH" title="MedGen record for Felty syndrome">Felty syndrome</a></span></li><li><span class="TLline"><a href="/medgen/220903" ref="tree=MeSH" title="MedGen record for Fetal akinesia deformation sequence 1">Fetal akinesia deformation sequence 1</a></span></li><li><span class="TLline"><a href="/medgen/4700" ref="tree=MeSH" title="MedGen record for Fibromuscular dysplasia">Fibromuscular dysplasia</a></span></li><li><span class="TLline"><a href="/medgen/152667" ref="tree=MeSH" title="MedGen record for Floating-Harbor syndrome">Floating-Harbor syndrome</a></span></li><li><span class="TLline"><a href="/medgen/42055" ref="tree=MeSH" title="MedGen record for Focal dermal hypoplasia">Focal dermal hypoplasia</a></span></li><li><span class="TLline"><a href="/medgen/8912" ref="tree=MeSH" title="MedGen record for Fragile X syndrome">Fragile X syndrome</a></span></li><li><span class="TLline"><a href="/medgen/5276" ref="tree=MeSH" title="MedGen record for Friedreich ataxia">Friedreich ataxia</a></span></li><li><span class="TLline"><a href="/medgen/406292" ref="tree=MeSH" title="MedGen record for Frontonasal dysplasia">Frontonasal dysplasia</a></span></li><li><span class="TLline"><a href="/medgen/83266" ref="tree=MeSH" title="MedGen record for Frontotemporal dementia">Frontotemporal dementia</a></span></li><li><span class="TLline"><a href="/medgen/65088" ref="tree=MeSH" title="MedGen record for Fryns syndrome">Fryns syndrome</a></span></li><li><span class="TLline"><a href="/medgen/4800" ref="tree=MeSH" title="MedGen record for Fuchs endothelial dystrophy">Fuchs endothelial dystrophy</a></span></li><li><span class="TLline"><a href="/medgen/473706" ref="tree=MeSH" title="MedGen record for G6PD deficiency">G6PD deficiency</a></span></li><li><span class="TLline"><a href="/medgen/167086" ref="tree=MeSH" title="MedGen record for Galloway-Mowat syndrome">Galloway-Mowat syndrome</a></span></li><li><span class="TLline"><a href="/medgen/1708537" ref="tree=MeSH" title="MedGen record for Gastrointestinal defect and immunodeficiency syndrome">Gastrointestinal defect and immunodeficiency syndrome</a></span></li><li><span class="TLline"><a href="/medgen/82721" ref="tree=MeSH" title="MedGen record for Gastroschisis">Gastroschisis</a></span></li><li><span class="TLline"><a href="/medgen/154257" ref="tree=MeSH" title="MedGen record for Genu varum">Genu varum</a></span></li><li><span class="TLline"><a href="/medgen/4886" ref="tree=MeSH" title="MedGen record for Gerstmann-Straussler-Scheinker syndrome">Gerstmann-Straussler-Scheinker syndrome</a></span></li><li><span class="TLline"><a href="/medgen/52736" ref="tree=MeSH" title="MedGen record for Glanzmann thrombasthenia">Glanzmann thrombasthenia</a></span></li><li><span class="TLline"><a href="/medgen/82889" ref="tree=MeSH" title="MedGen record for Glucocorticoid deficiency with achalasia">Glucocorticoid deficiency with achalasia</a></span></li><li><span class="TLline"><a href="/medgen/124337" ref="tree=MeSH" title="MedGen record for Glutaric aciduria, type 1">Glutaric aciduria, type 1</a></span></li><li><span class="TLline"><a href="/medgen/155625" ref="tree=MeSH" title="MedGen record for Glycine encephalopathy">Glycine encephalopathy</a></span></li><li><span class="TLline"><a href="/medgen/6639" ref="tree=MeSH" title="MedGen record for Glycogen storage disease">Glycogen storage disease</a></span></li><li><span class="TLline"><a href="/medgen/811223" ref="tree=MeSH" title="MedGen record for Granulomatosis with polyangiitis">Granulomatosis with polyangiitis</a></span></li><li><span class="TLline"><a href="/medgen/82900" ref="tree=MeSH" title="MedGen record for Gray platelet syndrome">Gray platelet syndrome</a></span></li><li><span class="TLline"><a href="/medgen/357030" ref="tree=MeSH" title="MedGen record for Griscelli syndrome type 2">Griscelli syndrome type 2</a></span></li><li><span class="TLline"><a href="/medgen/75683" ref="tree=MeSH" title="MedGen record for GTP cyclohydrolase I deficiency">GTP cyclohydrolase I deficiency</a></span></li><li><span class="TLline"><a href="/medgen/42316" ref="tree=MeSH" title="MedGen record for Gynatresia">Gynatresia</a></span></li><li><span class="TLline"><a href="/medgen/182961" ref="tree=MeSH" title="MedGen record for Hajdu-Cheney syndrome">Hajdu-Cheney syndrome</a></span></li><li><span class="TLline"><a href="/medgen/5414" ref="tree=MeSH" title="MedGen record for Hallermann-Streiff syndrome">Hallermann-Streiff syndrome</a></span></li><li><span class="TLline"><a href="/medgen/66205" ref="tree=MeSH" title="MedGen record for Hantavirus pulmonary syndrome">Hantavirus pulmonary syndrome</a></span></li><li><span class="TLline"><a href="/medgen/58162" ref="tree=MeSH" title="MedGen record for HELLP syndrome">HELLP syndrome</a></span></li><li><span class="TLline"><a href="/medgen/6158" ref="tree=MeSH" title="MedGen record for Hemophagocytic lymphohistiocytosis">Hemophagocytic lymphohistiocytosis</a></span></li><li><span class="TLline"><a href="/medgen/42408" ref="tree=MeSH" title="MedGen record for Hemorrhagic fever-renal syndrome">Hemorrhagic fever-renal syndrome</a></span></li><li><span class="TLline"><a href="/medgen/66355" ref="tree=MeSH" title="MedGen record for Hereditary acrodermatitis enteropathica">Hereditary acrodermatitis enteropathica</a></span></li><li><span class="TLline"><a href="/medgen/9229" ref="tree=MeSH" title="MedGen record for Hereditary angioneurotic edema">Hereditary angioneurotic edema</a></span></li><li><span class="TLline"><a href="/medgen/75781" ref="tree=MeSH" title="MedGen record for Hereditary antithrombin deficiency">Hereditary antithrombin deficiency</a></span></li><li><span class="TLline"><a href="/medgen/57931" ref="tree=MeSH" title="MedGen record for Hereditary coproporphyria">Hereditary coproporphyria</a></span></li><li><span class="TLline"><a href="/medgen/42105" ref="tree=MeSH" title="MedGen record for Hereditary fructosuria">Hereditary fructosuria</a></span></li><li><span class="TLline"><a href="/medgen/140272" ref="tree=MeSH" title="MedGen record for Hereditary hemochromatosis">Hereditary hemochromatosis</a></span></li><li><span class="TLline"><a href="/medgen/6963" ref="tree=MeSH" title="MedGen record for Hereditary hyperbilirubinemia">Hereditary hyperbilirubinemia</a></span></li><li><span class="TLline"><a href="/medgen/6915" ref="tree=MeSH" title="MedGen record for Hereditary insensitivity to pain with anhidrosis">Hereditary insensitivity to pain with anhidrosis</a></span></li><li><span class="TLline"><a href="/medgen/472940" ref="tree=MeSH" title="MedGen record for Hereditary orotic aciduria">Hereditary orotic aciduria</a></span></li><li><span class="TLline"><a href="/medgen/5495" ref="tree=MeSH" title="MedGen record for Hereditary persistence of fetal hemoglobin">Hereditary persistence of fetal hemoglobin</a></span></li><li><span class="TLline"><a href="/medgen/5645" ref="tree=MeSH" title="MedGen record for Hereditary sensory and autonomic neuropathy type 1">Hereditary sensory and autonomic neuropathy type 1</a></span></li><li><span class="TLline"><a href="/medgen/816212" ref="tree=MeSH" title="MedGen record for Hereditary sensory and autonomic neuropathy type 7">Hereditary sensory and autonomic neuropathy type 7</a></span></li><li><span class="TLline"><a href="/medgen/321945" ref="tree=MeSH" title="MedGen record for Hereditary thrombocytopenia and hematological cancer predisposition syndrome associated with RUNX1">Hereditary thrombocytopenia and hematological cancer predisposition syndrome associated with RUNX1</a></span></li><li><span class="TLline"><a href="/medgen/90953" ref="tree=MeSH" title="MedGen record for Heritable pulmonary arterial hypertension">Heritable pulmonary arterial hypertension</a></span></li><li><span class="TLline"><a href="/medgen/36313" ref="tree=MeSH" title="MedGen record for Hermansky-Pudlak syndrome">Hermansky-Pudlak syndrome</a></span></li><li><span class="TLline"><a href="/medgen/9233" ref="tree=MeSH" title="MedGen record for Herpes gestationis">Herpes gestationis</a></span></li><li><span class="TLline"><a href="/medgen/75780" ref="tree=MeSH" title="MedGen record for High molecular weight kininogen deficiency">High molecular weight kininogen deficiency</a></span></li><li><span class="TLline"><a href="/medgen/138" ref="tree=MeSH" title="MedGen record for Holmes-Adie syndrome">Holmes-Adie syndrome</a></span></li><li><span class="TLline"><a href="/medgen/120653" ref="tree=MeSH" title="MedGen record for Holocarboxylase synthetase deficiency">Holocarboxylase synthetase deficiency</a></span></li><li><span class="TLline"><a href="/medgen/38214" ref="tree=MeSH" title="MedGen record for Holoprosencephaly sequence">Holoprosencephaly sequence</a></span></li><li><span class="TLline"><a href="/medgen/340382" ref="tree=MeSH" title="MedGen record for Holoprosencephaly-postaxial polydactyly syndrome">Holoprosencephaly-postaxial polydactyly syndrome</a></span></li><li><span class="TLline"><a href="/medgen/120524" ref="tree=MeSH" title="MedGen record for Holt-Oram syndrome">Holt-Oram syndrome</a></span></li><li><span class="TLline"><a href="/medgen/42485" ref="tree=MeSH" title="MedGen record for Homocystinuria">Homocystinuria</a></span></li><li><span class="TLline"><a href="/medgen/46123" ref="tree=MeSH" title="MedGen record for Hutchinson-Gilford syndrome">Hutchinson-Gilford syndrome</a></span></li><li><span class="TLline"><a href="/medgen/235180" ref="tree=MeSH" title="MedGen record for Hyaline Membrane Syndrome">Hyaline Membrane Syndrome</a></span></li><li><span class="TLline"><a href="/medgen/5661" ref="tree=MeSH" title="MedGen record for Hydroa vacciniforme">Hydroa vacciniforme</a></span></li><li><span class="TLline"><a href="/medgen/6947" ref="tree=MeSH" title="MedGen record for Hydrops fetalis">Hydrops fetalis</a></span></li><li><span class="TLline"><a href="/medgen/43772" ref="tree=MeSH" title="MedGen record for Hymenolepiasis">Hymenolepiasis</a></span></li><li><span class="TLline"><a href="/medgen/120649" ref="tree=MeSH" title="MedGen record for Hyperammonemia, type III">Hyperammonemia, type III</a></span></li><li><span class="TLline"><a href="/medgen/1651776" ref="tree=MeSH" title="MedGen record for HyperCKmia">HyperCKmia</a></span></li><li><span class="TLline"><a href="/medgen/68665" ref="tree=MeSH" title="MedGen record for Hyperkalemic periodic paralysis">Hyperkalemic periodic paralysis</a></span></li><li><span class="TLline"><a href="/medgen/7352" ref="tree=MeSH" title="MedGen record for Hyperlipoproteinemia, type I">Hyperlipoproteinemia, type I</a></span></li><li><span class="TLline"><a href="/medgen/82815" ref="tree=MeSH" title="MedGen record for Hyperornithinemia-hyperammonemia-homocitrullinuria syndrome">Hyperornithinemia-hyperammonemia-homocitrullinuria syndrome</a></span></li><li><span class="TLline"><a href="/medgen/57890" ref="tree=MeSH" title="MedGen record for Hypohidrotic X-linked ectodermal dysplasia">Hypohidrotic X-linked ectodermal dysplasia</a></span></li><li><span class="TLline"><a href="/medgen/116058" ref="tree=MeSH" title="MedGen record for Hypokalemic periodic paralysis">Hypokalemic periodic paralysis</a></span></li><li><span class="TLline"><a href="/medgen/340984" ref="tree=MeSH" title="MedGen record for Hypoparathyroidism-retardation-dysmorphism syndrome">Hypoparathyroidism-retardation-dysmorphism syndrome</a></span></li><li><span class="TLline"><a href="/medgen/140809" ref="tree=MeSH" title="MedGen record for Hypoplastic enamel-onycholysis-hypohidrosis syndrome">Hypoplastic enamel-onycholysis-hypohidrosis syndrome</a></span></li><li><span class="TLline"><a href="/medgen/1792034" ref="tree=MeSH" title="MedGen record for Idiopathic Basal Ganglia Calcification">Idiopathic Basal Ganglia Calcification</a></span></li><li><span class="TLline"><a href="/medgen/1637664" ref="tree=MeSH" title="MedGen record for Idiopathic basal ganglia calcification 1">Idiopathic basal ganglia calcification 1</a></span></li><li><span class="TLline"><a href="/medgen/64647" ref="tree=MeSH" title="MedGen record for Idiopathic CD4-positive T-lymphocytopenia">Idiopathic CD4-positive T-lymphocytopenia</a></span></li><li><span class="TLline"><a href="/medgen/155626" ref="tree=MeSH" title="MedGen record for Idiopathic hypersomnia">Idiopathic hypersomnia</a></span></li><li><span class="TLline"><a href="/medgen/419725" ref="tree=MeSH" title="MedGen record for IgAD1">IgAD1</a></span></li><li><span class="TLline"><a href="/medgen/1636193" ref="tree=MeSH" title="MedGen record for Immunodeficiency-centromeric instability-facial anomalies syndrome 1">Immunodeficiency-centromeric instability-facial anomalies syndrome 1</a></span></li><li><span class="TLline"><a href="/medgen/1997" ref="tree=MeSH" title="MedGen record for Imperforate anus">Imperforate anus</a></span></li><li><span class="TLline"><a href="/medgen/539901" ref="tree=MeSH" title="MedGen record for Imperforate Vagina">Imperforate Vagina</a></span></li><li><span class="TLline"><a href="/medgen/82803" ref="tree=MeSH" title="MedGen record for Inborn glycerol kinase deficiency">Inborn glycerol kinase deficiency</a></span></li><li><span class="TLline"><a href="/medgen/7049" ref="tree=MeSH" title="MedGen record for Incontinentia pigmenti syndrome">Incontinentia pigmenti syndrome</a></span></li><li><span class="TLline"><a href="/medgen/43781" ref="tree=MeSH" title="MedGen record for Infantile cortical hyperostosis">Infantile cortical hyperostosis</a></span></li><li><span class="TLline"><a href="/medgen/82852" ref="tree=MeSH" title="MedGen record for Infantile neuroaxonal dystrophy">Infantile neuroaxonal dystrophy</a></span></li><li><span class="TLline"><a href="/medgen/21645" ref="tree=MeSH" title="MedGen record for Infection by larvae of Trichinella">Infection by larvae of Trichinella</a></span></li><li><span class="TLline"><a href="/medgen/14603" ref="tree=MeSH" title="MedGen record for Infection by Paragonimus">Infection by Paragonimus</a></span></li><li><span class="TLline"><a href="/medgen/452450" ref="tree=MeSH" title="MedGen record for Inosine triphosphatase deficiency">Inosine triphosphatase deficiency</a></span></li><li><span class="TLline"><a href="/medgen/409857" ref="tree=MeSH" title="MedGen record for Intellectual disability, autosomal dominant 1">Intellectual disability, autosomal dominant 1</a></span></li><li><span class="TLline"><a href="/medgen/909304" ref="tree=MeSH" title="MedGen record for Intellectual disability, autosomal dominant 39">Intellectual disability, autosomal dominant 39</a></span></li><li><span class="TLline"><a href="/medgen/482674" ref="tree=MeSH" title="MedGen record for Intellectual disability, autosomal recessive 34">Intellectual disability, autosomal recessive 34</a></span></li><li><span class="TLline"><a href="/medgen/444070" ref="tree=MeSH" title="MedGen record for Intellectual disability, X-linked 1">Intellectual disability, X-linked 1</a></span></li><li><span class="TLline"><a href="/medgen/7129" ref="tree=MeSH" title="MedGen record for Intestinal atresia">Intestinal atresia</a></span></li><li><span class="TLline"><a href="/medgen/242751" ref="tree=MeSH" title="MedGen record for Iridocorneal endothelial syndrome">Iridocorneal endothelial syndrome</a></span></li><li><span class="TLline"><a href="/medgen/19310" ref="tree=MeSH" title="MedGen record for Isolated Pierre-Robin syndrome">Isolated Pierre-Robin syndrome</a></span></li><li><span class="TLline"><a href="/medgen/208653" ref="tree=MeSH" title="MedGen record for Jackson-Weiss syndrome">Jackson-Weiss syndrome</a></span></li><li><span class="TLline"><a href="/medgen/5929" ref="tree=MeSH" title="MedGen record for Jervell and Lange-Nielsen syndrome">Jervell and Lange-Nielsen syndrome</a></span></li><li><span class="TLline"><a href="/medgen/78548" ref="tree=MeSH" title="MedGen record for Jeune thoracic dystrophy">Jeune thoracic dystrophy</a></span></li><li><span class="TLline"><a href="/medgen/162897" ref="tree=MeSH" title="MedGen record for Kabuki syndrome">Kabuki syndrome</a></span></li><li><span class="TLline"><a href="/medgen/9618" ref="tree=MeSH" title="MedGen record for Kearns-Sayre syndrome">Kearns-Sayre syndrome</a></span></li><li><span class="TLline"><a href="/medgen/333282" ref="tree=MeSH" title="MedGen record for Kennedy disease">Kennedy disease</a></span></li><li><span class="TLline"><a href="/medgen/5956" ref="tree=MeSH" title="MedGen record for Keratosis follicularis">Keratosis follicularis</a></span></li><li><span class="TLline"><a href="/medgen/46183" ref="tree=MeSH" title="MedGen record for Kimura disease">Kimura disease</a></span></li><li><span class="TLline"><a href="/medgen/208639" ref="tree=MeSH" title="MedGen record for Kleefstra syndrome 1">Kleefstra syndrome 1</a></span></li><li><span class="TLline"><a href="/medgen/61511" ref="tree=MeSH" title="MedGen record for Kleine-Levin syndrome">Kleine-Levin syndrome</a></span></li><li><span class="TLline"><a href="/medgen/9645" ref="tree=MeSH" title="MedGen record for Klippel-Feil syndrome">Klippel-Feil syndrome</a></span></li><li><span class="TLline"><a href="/medgen/124361" ref="tree=MeSH" title="MedGen record for Kluver-Bucy syndrome">Kluver-Bucy syndrome</a></span></li><li><span class="TLline"><a href="/medgen/75559" ref="tree=MeSH" title="MedGen record for Kniest dysplasia">Kniest dysplasia</a></span></li><li><span class="TLline"><a href="/medgen/155631" ref="tree=MeSH" title="MedGen record for Lafora disease">Lafora disease</a></span></li><li><span class="TLline"><a href="/medgen/79465" ref="tree=MeSH" title="MedGen record for Landau-Kleffner syndrome">Landau-Kleffner syndrome</a></span></li><li><span class="TLline"><a href="/medgen/6009" ref="tree=MeSH" title="MedGen record for Langer-Giedion syndrome">Langer-Giedion syndrome</a></span></li><li><span class="TLline"><a href="/medgen/53057" ref="tree=MeSH" title="MedGen record for Lateral medullary syndrome">Lateral medullary syndrome</a></span></li><li><span class="TLline"><a href="/medgen/137922" ref="tree=MeSH" title="MedGen record for Leber congenital amaurosis">Leber congenital amaurosis</a></span></li><li><span class="TLline"><a href="/medgen/182973" ref="tree=MeSH" title="MedGen record for Leber optic atrophy">Leber optic atrophy</a></span></li><li><span class="TLline"><a href="/medgen/44095" ref="tree=MeSH" title="MedGen record for Leigh disease">Leigh disease</a></span></li><li><span class="TLline"><a href="/medgen/116044" ref="tree=MeSH" title="MedGen record for Lennox-Gastaut syndrome">Lennox-Gastaut syndrome</a></span></li><li><span class="TLline"><a href="/medgen/82708" ref="tree=MeSH" title="MedGen record for Leprechaunism syndrome">Leprechaunism syndrome</a></span></li><li><span class="TLline"><a href="/medgen/6049" ref="tree=MeSH" title="MedGen record for Leprosy">Leprosy</a></span></li><li><span class="TLline"><a href="/medgen/7309" ref="tree=MeSH" title="MedGen record for Leptospirosis">Leptospirosis</a></span></li><li><span class="TLline"><a href="/medgen/75562" ref="tree=MeSH" title="MedGen record for Leri-Weill dyschondrosteosis">Leri-Weill dyschondrosteosis</a></span></li><li><span class="TLline"><a href="/medgen/9721" ref="tree=MeSH" title="MedGen record for Lesch-Nyhan syndrome">Lesch-Nyhan syndrome</a></span></li><li><span class="TLline"><a href="/medgen/1638681" ref="tree=MeSH" title="MedGen record for Leukoencephalopathy with mild cerebellar ataxia and white matter edema">Leukoencephalopathy with mild cerebellar ataxia and white matter edema</a></span></li><li><span class="TLline"><a href="/medgen/67439" ref="tree=MeSH" title="MedGen record for Liddle syndrome">Liddle syndrome</a></span></li><li><span class="TLline"><a href="/medgen/340886" ref="tree=MeSH" title="MedGen record for Lipase deficiency, combined">Lipase deficiency, combined</a></span></li><li><span class="TLline"><a href="/medgen/6112" ref="tree=MeSH" title="MedGen record for Lipid proteinosis">Lipid proteinosis</a></span></li><li><span class="TLline"><a href="/medgen/1757" ref="tree=MeSH" title="MedGen record for Lipomatosis dolorosa">Lipomatosis dolorosa</a></span></li><li><span class="TLline"><a href="/medgen/78604" ref="tree=MeSH" title="MedGen record for Lissencephaly">Lissencephaly</a></span></li><li><span class="TLline"><a href="/medgen/395827" ref="tree=MeSH" title="MedGen record for Loeys-Dietz syndrome">Loeys-Dietz syndrome</a></span></li><li><span class="TLline"><a href="/medgen/778253" ref="tree=MeSH" title="MedGen record for Long chain 3-hydroxyacyl-CoA dehydrogenase deficiency">Long chain 3-hydroxyacyl-CoA dehydrogenase deficiency</a></span></li><li><span class="TLline"><a href="/medgen/65087" ref="tree=MeSH" title="MedGen record for Long chain acyl-CoA dehydrogenase deficiency">Long chain acyl-CoA dehydrogenase deficiency</a></span></li><li><span class="TLline"><a href="/medgen/18145" ref="tree=MeSH" title="MedGen record for Lowe syndrome">Lowe syndrome</a></span></li><li><span class="TLline"><a href="/medgen/75704" ref="tree=MeSH" title="MedGen record for Lysinuric protein intolerance">Lysinuric protein intolerance</a></span></li><li><span class="TLline"><a href="/medgen/43098" ref="tree=MeSH" title="MedGen record for Lysosomal storage disease">Lysosomal storage disease</a></span></li><li><span class="TLline"><a href="/medgen/1704278" ref="tree=MeSH" title="MedGen record for Macrothrombocytopenia and granulocyte inclusions with or without nephritis or sensorineural hearing loss">Macrothrombocytopenia and granulocyte inclusions with or without nephritis or sensorineural hearing loss</a></span></li><li><span class="TLline"><a href="/medgen/44257" ref="tree=MeSH" title="MedGen record for Malakoplakia">Malakoplakia</a></span></li><li><span class="TLline"><a href="/medgen/364975" ref="tree=MeSH" title="MedGen record for Malformation of cortical development">Malformation of cortical development</a></span></li><li><span class="TLline"><a href="/medgen/113138" ref="tree=MeSH" title="MedGen record for Malignant atrophic papulosis">Malignant atrophic papulosis</a></span></li><li><span class="TLline"><a href="/medgen/9867" ref="tree=MeSH" title="MedGen record for Malignant hyperthermia of anesthesia">Malignant hyperthermia of anesthesia</a></span></li><li><span class="TLline"><a href="/medgen/782160" ref="tree=MeSH" title="MedGen record for Malignant migrating partial seizures of infancy">Malignant migrating partial seizures of infancy</a></span></li><li><span class="TLline"><a href="/medgen/44265" ref="tree=MeSH" title="MedGen record for Mallory-Weiss syndrome">Mallory-Weiss syndrome</a></span></li><li><span class="TLline"><a href="/medgen/1757618" ref="tree=MeSH" title="MedGen record for Mandibuloacral dysplasia with type A lipodystrophy">Mandibuloacral dysplasia with type A lipodystrophy</a></span></li><li><span class="TLline"><a href="/medgen/6213" ref="tree=MeSH" title="MedGen record for Mansonelliasis">Mansonelliasis</a></span></li><li><span class="TLline"><a href="/medgen/6217" ref="tree=MeSH" title="MedGen record for Maple syrup urine disease">Maple syrup urine disease</a></span></li><li><span class="TLline"><a href="/medgen/9888" ref="tree=MeSH" title="MedGen record for Marburg virus disease">Marburg virus disease</a></span></li><li><span class="TLline"><a href="/medgen/44287" ref="tree=MeSH" title="MedGen record for Marfan syndrome">Marfan syndrome</a></span></li><li><span class="TLline"><a href="/medgen/82694" ref="tree=MeSH" title="MedGen record for Marshall syndrome">Marshall syndrome</a></span></li><li><span class="TLline"><a href="/medgen/162894" ref="tree=MeSH" title="MedGen record for MASA syndrome">MASA syndrome</a></span></li><li><span class="TLline"><a href="/medgen/120513" ref="tree=MeSH" title="MedGen record for Meckel-Gruber syndrome">Meckel-Gruber syndrome</a></span></li><li><span class="TLline"><a href="/medgen/65086" ref="tree=MeSH" title="MedGen record for Medium-chain acyl-coenzyme A dehydrogenase deficiency">Medium-chain acyl-coenzyme A dehydrogenase deficiency</a></span></li><li><span class="TLline"><a href="/medgen/83283" ref="tree=MeSH" title="MedGen record for Meesmann corneal dystrophy">Meesmann corneal dystrophy</a></span></li><li><span class="TLline"><a href="/medgen/296125" ref="tree=MeSH" title="MedGen record for Megacystis, microcolon, hypoperistalsis syndrome">Megacystis, microcolon, hypoperistalsis syndrome</a></span></li><li><span class="TLline"><a href="/medgen/56485" ref="tree=MeSH" title="MedGen record for MELAS syndrome">MELAS syndrome</a></span></li><li><span class="TLline"><a href="/medgen/6291" ref="tree=MeSH" title="MedGen record for Melkersson-Rosenthal syndrome">Melkersson-Rosenthal syndrome</a></span></li><li><span class="TLline"><a href="/medgen/1781109" ref="tree=MeSH" title="MedGen record for Mendelian susceptibility to mycobacterial disease">Mendelian susceptibility to mycobacterial disease</a></span></li><li><span class="TLline"><a href="/medgen/44030" ref="tree=MeSH" title="MedGen record for Menkes kinky-hair syndrome">Menkes kinky-hair syndrome</a></span></li><li><span class="TLline"><a href="/medgen/894460" ref="tree=MeSH" title="MedGen record for Mental Retardation, Autosomal Dominant 40">Mental Retardation, Autosomal Dominant 40</a></span></li><li><span class="TLline"><a href="/medgen/897961" ref="tree=MeSH" title="MedGen record for Mental Retardation, X-linked 102">Mental Retardation, X-linked 102</a></span></li><li><span class="TLline"><a href="/medgen/56486" ref="tree=MeSH" title="MedGen record for MERRF syndrome">MERRF syndrome</a></span></li><li><span class="TLline"><a href="/medgen/120529" ref="tree=MeSH" title="MedGen record for Metaphyseal chondrodysplasia, Jansen type">Metaphyseal chondrodysplasia, Jansen type</a></span></li><li><span class="TLline"><a href="/medgen/67398" ref="tree=MeSH" title="MedGen record for Metaphyseal chondrodysplasia, McKusick type">Metaphyseal chondrodysplasia, McKusick type</a></span></li><li><span class="TLline"><a href="/medgen/82699" ref="tree=MeSH" title="MedGen record for Metatropic dysplasia">Metatropic dysplasia</a></span></li><li><span class="TLline"><a href="/medgen/120654" ref="tree=MeSH" title="MedGen record for Methylmalonic acidemia">Methylmalonic acidemia</a></span></li><li><span class="TLline"><a href="/medgen/480111" ref="tree=MeSH" title="MedGen record for Microcephaly and chorioretinopathy 1">Microcephaly and chorioretinopathy 1</a></span></li><li><span class="TLline"><a href="/medgen/1377952" ref="tree=MeSH" title="MedGen record for Mitochondrial DNA depletion syndrome 12">Mitochondrial DNA depletion syndrome 12</a></span></li><li><span class="TLline"><a href="/medgen/815922" ref="tree=MeSH" title="MedGen record for Mitochondrial DNA depletion syndrome 13">Mitochondrial DNA depletion syndrome 13</a></span></li><li><span class="TLline"><a href="/medgen/167876" ref="tree=MeSH" title="MedGen record for Mitochondrial neurogastrointestinal encephalomyopathy">Mitochondrial neurogastrointestinal encephalomyopathy</a></span></li><li><span class="TLline"><a href="/medgen/370665" ref="tree=MeSH" title="MedGen record for Mitochondrial trifunctional protein deficiency">Mitochondrial trifunctional protein deficiency</a></span></li><li><span class="TLline"><a href="/medgen/1651816" ref="tree=MeSH" title="MedGen record for Mitochondrially Inherited Nonsyndromic Sensorineural Deafness">Mitochondrially Inherited Nonsyndromic Sensorineural Deafness</a></span></li><li><span class="TLline"><a href="/medgen/10069" ref="tree=MeSH" title="MedGen record for Mixed connective tissue disease">Mixed connective tissue disease</a></span></li><li><span class="TLline"><a href="/medgen/418947" ref="tree=MeSH" title="MedGen record for Mosaic trisomy 14">Mosaic trisomy 14</a></span></li><li><span class="TLline"><a href="/medgen/341067" ref="tree=MeSH" title="MedGen record for Mowat-Wilson syndrome">Mowat-Wilson syndrome</a></span></li><li><span class="TLline"><a href="/medgen/7726" ref="tree=MeSH" title="MedGen record for Moyamoya disease">Moyamoya disease</a></span></li><li><span class="TLline"><a href="/medgen/355217" ref="tree=MeSH" title="MedGen record for Muenke syndrome">Muenke syndrome</a></span></li><li><span class="TLline"><a href="/medgen/99347" ref="tree=MeSH" title="MedGen record for Mulibrey nanism syndrome">Mulibrey nanism syndrome</a></span></li><li><span class="TLline"><a href="/medgen/543458" ref="tree=MeSH" title="MedGen record for Mullerian inhibiting factor deficiency">Mullerian inhibiting factor deficiency</a></span></li><li><span class="TLline"><a href="/medgen/436237" ref="tree=MeSH" title="MedGen record for Multicentric carpo-tarsal osteolysis with or without nephropathy">Multicentric carpo-tarsal osteolysis with or without nephropathy</a></span></li><li><span class="TLline"><a href="/medgen/342428" ref="tree=MeSH" title="MedGen record for Multicentric osteolysis nodulosis arthropathy spectrum">Multicentric osteolysis nodulosis arthropathy spectrum</a></span></li><li><span class="TLline"><a href="/medgen/75696" ref="tree=MeSH" title="MedGen record for Multiple acyl-CoA dehydrogenase deficiency">Multiple acyl-CoA dehydrogenase deficiency</a></span></li><li><span class="TLline"><a href="/medgen/98276" ref="tree=MeSH" title="MedGen record for Multiple system atrophy">Multiple system atrophy</a></span></li><li><span class="TLline"><a href="/medgen/44527" ref="tree=MeSH" title="MedGen record for Muscular dystrophy">Muscular dystrophy</a></span></li><li><span class="TLline"><a href="/medgen/167103" ref="tree=MeSH" title="MedGen record for Myhre syndrome">Myhre syndrome</a></span></li><li><span class="TLline"><a href="/medgen/146882" ref="tree=MeSH" title="MedGen record for Myokymia">Myokymia</a></span></li><li><span class="TLline"><a href="/medgen/44564" ref="tree=MeSH" title="MedGen record for Myositis disease">Myositis disease</a></span></li><li><span class="TLline"><a href="/medgen/107510" ref="tree=MeSH" title="MedGen record for Myotonic syndrome">Myotonic syndrome</a></span></li><li><span class="TLline"><a href="/medgen/476133" ref="tree=MeSH" title="MedGen record for NADH Dehydrogenase Deficiency">NADH Dehydrogenase Deficiency</a></span></li><li><span class="TLline"><a href="/medgen/10257" ref="tree=MeSH" title="MedGen record for Nail-patella syndrome">Nail-patella syndrome</a></span></li><li><span class="TLline"><a href="/medgen/6544" ref="tree=MeSH" title="MedGen record for Nelson Syndrome">Nelson Syndrome</a></span></li><li><span class="TLline"><a href="/medgen/140806" ref="tree=MeSH" title="MedGen record for Neonatal pseudo-hydrocephalic progeroid syndrome">Neonatal pseudo-hydrocephalic progeroid syndrome</a></span></li><li><span class="TLline"><a href="/medgen/482659" ref="tree=MeSH" title="MedGen record for Neonatal-onset encephalopathy with rigidity and seizures">Neonatal-onset encephalopathy with rigidity and seizures</a></span></li><li><span class="TLline"><a href="/medgen/10222" ref="tree=MeSH" title="MedGen record for Nephrocalcinosis">Nephrocalcinosis</a></span></li><li><span class="TLline"><a href="/medgen/301436" ref="tree=MeSH" title="MedGen record for Nephrogenic fibrosing dermopathy">Nephrogenic fibrosing dermopathy</a></span></li><li><span class="TLline"><a href="/medgen/18009" ref="tree=MeSH" title="MedGen record for Neural tube defect">Neural tube defect</a></span></li><li><span class="TLline"><a href="/medgen/482001" ref="tree=MeSH" title="MedGen record for Neurodegeneration with brain iron accumulation 4">Neurodegeneration with brain iron accumulation 4</a></span></li><li><span class="TLline"><a href="/medgen/763887" ref="tree=MeSH" title="MedGen record for Neurodegeneration with brain iron accumulation 5">Neurodegeneration with brain iron accumulation 5</a></span></li><li><span class="TLline"><a href="/medgen/45063" ref="tree=MeSH" title="MedGen record for Neuromyelitis optica">Neuromyelitis optica</a></span></li><li><span class="TLline"><a href="/medgen/6723" ref="tree=MeSH" title="MedGen record for Neutral 1 amino acid transport defect">Neutral 1 amino acid transport defect</a></span></li><li><span class="TLline"><a href="/medgen/415589" ref="tree=MeSH" title="MedGen record for Non-Trisomic Autosomal Aneuploidy">Non-Trisomic Autosomal Aneuploidy</a></span></li><li><span class="TLline"><a href="/medgen/104494" ref="tree=MeSH" title="MedGen record for Noonan syndrome with multiple lentigines">Noonan syndrome with multiple lentigines</a></span></li><li><span class="TLline"><a href="/medgen/9698" ref="tree=MeSH" title="MedGen record for Norum disease">Norum disease</a></span></li><li><span class="TLline"><a href="/medgen/45177" ref="tree=MeSH" title="MedGen record for Ochronosis disorder">Ochronosis disorder</a></span></li><li><span class="TLline"><a href="/medgen/10435" ref="tree=MeSH" title="MedGen record for Olivopontocerebellar atrophy">Olivopontocerebellar atrophy</a></span></li><li><span class="TLline"><a href="/medgen/854546" ref="tree=MeSH" title="MedGen record for Optic neuropathy">Optic neuropathy</a></span></li><li><span class="TLline"><a href="/medgen/349303" ref="tree=MeSH" title="MedGen record for Orofacial cleft 1">Orofacial cleft 1</a></span></li><li><span class="TLline"><a href="/medgen/307142" ref="tree=MeSH" title="MedGen record for Orofaciodigital syndrome I">Orofaciodigital syndrome I</a></span></li><li><span class="TLline"><a href="/medgen/411200" ref="tree=MeSH" title="MedGen record for Orofaciodigital syndrome type 6">Orofaciodigital syndrome type 6</a></span></li><li><span class="TLline"><a href="/medgen/66357" ref="tree=MeSH" title="MedGen record for Oromandibular-limb hypogenesis spectrum">Oromandibular-limb hypogenesis spectrum</a></span></li><li><span class="TLline"><a href="/medgen/104849" ref="tree=MeSH" title="MedGen record for Ossification of posterior longitudinal ligament">Ossification of posterior longitudinal ligament</a></span></li><li><span class="TLline"><a href="/medgen/10495" ref="tree=MeSH" title="MedGen record for Osteochondrodysplasia">Osteochondrodysplasia</a></span></li><li><span class="TLline"><a href="/medgen/91042" ref="tree=MeSH" title="MedGen record for Osteopetrosis with renal tubular acidosis">Osteopetrosis with renal tubular acidosis</a></span></li><li><span class="TLline"><a href="/medgen/45251" ref="tree=MeSH" title="MedGen record for Osteopoikilosis">Osteopoikilosis</a></span></li><li><span class="TLline"><a href="/medgen/78542" ref="tree=MeSH" title="MedGen record for Oto-palato-digital syndrome, type I">Oto-palato-digital syndrome, type I</a></span></li><li><span class="TLline"><a href="/medgen/18210" ref="tree=MeSH" title="MedGen record for Pachydermoperiostosis syndrome">Pachydermoperiostosis syndrome</a></span></li><li><span class="TLline"><a href="/medgen/78556" ref="tree=MeSH" title="MedGen record for Pachyonychia congenita syndrome">Pachyonychia congenita syndrome</a></span></li><li><span class="TLline"><a href="/medgen/154351" ref="tree=MeSH" title="MedGen record for Pain agnosia">Pain agnosia</a></span></li><li><span class="TLline"><a href="/medgen/120540" ref="tree=MeSH" title="MedGen record for Pallister-Killian syndrome">Pallister-Killian syndrome</a></span></li><li><span class="TLline"><a href="/medgen/482157" ref="tree=MeSH" title="MedGen record for Pancreatic triacylglycerol lipase deficiency">Pancreatic triacylglycerol lipase deficiency</a></span></li><li><span class="TLline"><a href="/medgen/45303" ref="tree=MeSH" title="MedGen record for Panuveitis">Panuveitis</a></span></li><li><span class="TLline"><a href="/medgen/45306" ref="tree=MeSH" title="MedGen record for Papillon-Lefèvre syndrome">Papillon-Lefèvre syndrome</a></span></li><li><span class="TLline"><a href="/medgen/331565" ref="tree=MeSH" title="MedGen record for Paroxysmal extreme pain disorder">Paroxysmal extreme pain disorder</a></span></li><li><span class="TLline"><a href="/medgen/87459" ref="tree=MeSH" title="MedGen record for Pearson syndrome">Pearson syndrome</a></span></li><li><span class="TLline"><a href="/medgen/10617" ref="tree=MeSH" title="MedGen record for Pelger-Huët anomaly">Pelger-Huët anomaly</a></span></li><li><span class="TLline"><a href="/medgen/61440" ref="tree=MeSH" title="MedGen record for Pelizaeus-Merzbacher disease">Pelizaeus-Merzbacher disease</a></span></li><li><span class="TLline"><a href="/medgen/107540" ref="tree=MeSH" title="MedGen record for Pentalogy of Cantrell">Pentalogy of Cantrell</a></span></li><li><span class="TLline"><a href="/medgen/10560" ref="tree=MeSH" title="MedGen record for Peritoneal Panniculitis">Peritoneal Panniculitis</a></span></li><li><span class="TLline"><a href="/medgen/45824" ref="tree=MeSH" title="MedGen record for Persistent fetal circulation syndrome">Persistent fetal circulation syndrome</a></span></li><li><span class="TLline"><a href="/medgen/163204" ref="tree=MeSH" title="MedGen record for Peters plus syndrome">Peters plus syndrome</a></span></li><li><span class="TLline"><a href="/medgen/162924" ref="tree=MeSH" title="MedGen record for Pettigrew syndrome">Pettigrew syndrome</a></span></li><li><span class="TLline"><a href="/medgen/339994" ref="tree=MeSH" title="MedGen record for Phelan-McDermid syndrome">Phelan-McDermid syndrome</a></span></li><li><span class="TLline"><a href="/medgen/120618" ref="tree=MeSH" title="MedGen record for Phosphoenolpyruvate carboxykinase (GTP) deficiency">Phosphoenolpyruvate carboxykinase (GTP) deficiency</a></span></li><li><span class="TLline"><a href="/medgen/116020" ref="tree=MeSH" title="MedGen record for Pick disease">Pick disease</a></span></li><li><span class="TLline"><a href="/medgen/36361" ref="tree=MeSH" title="MedGen record for Piebaldism">Piebaldism</a></span></li><li><span class="TLline"><a href="/medgen/6708" ref="tree=MeSH" title="MedGen record for Pigmentary pallidal degeneration">Pigmentary pallidal degeneration</a></span></li><li><span class="TLline"><a href="/medgen/1790024" ref="tree=MeSH" title="MedGen record for PIK3CA related overgrowth syndrome">PIK3CA related overgrowth syndrome</a></span></li><li><span class="TLline"><a href="/medgen/1784355" ref="tree=MeSH" title="MedGen record for PIK3R1 Deficiency">PIK3R1 Deficiency</a></span></li><li><span class="TLline"><a href="/medgen/45926" ref="tree=MeSH" title="MedGen record for Pinta disease">Pinta disease</a></span></li><li><span class="TLline"><a href="/medgen/141601" ref="tree=MeSH" title="MedGen record for Piriformis syndrome">Piriformis syndrome</a></span></li><li><span class="TLline"><a href="/medgen/10785" ref="tree=MeSH" title="MedGen record for Plague">Plague</a></span></li><li><span class="TLline"><a href="/medgen/1387546" ref="tree=MeSH" title="MedGen record for Plasma Kallikrein Deficiency">Plasma Kallikrein Deficiency</a></span></li><li><span class="TLline"><a href="/medgen/396078" ref="tree=MeSH" title="MedGen record for Platelet-type bleeding disorder 17">Platelet-type bleeding disorder 17</a></span></li><li><span class="TLline"><a href="/medgen/45967" ref="tree=MeSH" title="MedGen record for Plummer-Vinson syndrome">Plummer-Vinson syndrome</a></span></li><li><span class="TLline"><a href="/medgen/388129" ref="tree=MeSH" title="MedGen record for Poikiloderma with neutropenia">Poikiloderma with neutropenia</a></span></li><li><span class="TLline"><a href="/medgen/10822" ref="tree=MeSH" title="MedGen record for Poland anomaly">Poland anomaly</a></span></li><li><span class="TLline"><a href="/medgen/1680556" ref="tree=MeSH" title="MedGen record for POLG-Related Spectrum Disorders">POLG-Related Spectrum Disorders</a></span></li><li><span class="TLline"><a href="/medgen/78543" ref="tree=MeSH" title="MedGen record for Popliteal pterygium syndrome">Popliteal pterygium syndrome</a></span></li><li><span class="TLline"><a href="/medgen/78659" ref="tree=MeSH" title="MedGen record for Porphobilinogen synthase deficiency">Porphobilinogen synthase deficiency</a></span></li><li><span class="TLline"><a href="/medgen/56453" ref="tree=MeSH" title="MedGen record for Porphyria cutanea tarda">Porphyria cutanea tarda</a></span></li><li><span class="TLline"><a href="/medgen/444010" ref="tree=MeSH" title="MedGen record for Potocki-Lupski syndrome">Potocki-Lupski syndrome</a></span></li><li><span class="TLline"><a href="/medgen/318657" ref="tree=MeSH" title="MedGen record for Potocki-Shaffer syndrome">Potocki-Shaffer syndrome</a></span></li><li><span class="TLline"><a href="/medgen/75779" ref="tree=MeSH" title="MedGen record for Prekallikrein deficiency">Prekallikrein deficiency</a></span></li><li><span class="TLline"><a href="/medgen/3467" ref="tree=MeSH" title="MedGen record for Primary ciliary dyskinesia">Primary ciliary dyskinesia</a></span></li><li><span class="TLline"><a href="/medgen/183649" ref="tree=MeSH" title="MedGen record for Primary familial hypertrophic cardiomyopathy">Primary familial hypertrophic cardiomyopathy</a></span></li><li><span class="TLline"><a href="/medgen/57591" ref="tree=MeSH" title="MedGen record for Primary lateral sclerosis">Primary lateral sclerosis</a></span></li><li><span class="TLline"><a href="/medgen/79466" ref="tree=MeSH" title="MedGen record for Primary progressive aphasia">Primary progressive aphasia</a></span></li><li><span class="TLline"><a href="/medgen/18290" ref="tree=MeSH" title="MedGen record for Progressive bulbar palsy">Progressive bulbar palsy</a></span></li><li><span class="TLline"><a href="/medgen/214634" ref="tree=MeSH" title="MedGen record for Progressive muscular atrophy">Progressive muscular atrophy</a></span></li><li><span class="TLline"><a href="/medgen/4698" ref="tree=MeSH" title="MedGen record for Progressive myositis ossificans">Progressive myositis ossificans</a></span></li><li><span class="TLline"><a href="/medgen/21026" ref="tree=MeSH" title="MedGen record for Progressive supranuclear palsy">Progressive supranuclear palsy</a></span></li><li><span class="TLline"><a href="/medgen/120647" ref="tree=MeSH" title="MedGen record for Prolidase deficiency">Prolidase deficiency</a></span></li><li><span class="TLline"><a href="/medgen/65884" ref="tree=MeSH" title="MedGen record for Prosopagnosia">Prosopagnosia</a></span></li><li><span class="TLline"><a href="/medgen/39008" ref="tree=MeSH" title="MedGen record for Proteus syndrome">Proteus syndrome</a></span></li><li><span class="TLline"><a href="/medgen/18718" ref="tree=MeSH" title="MedGen record for Prune belly syndrome">Prune belly syndrome</a></span></li><li><span class="TLline"><a href="/medgen/98378" ref="tree=MeSH" title="MedGen record for Pseudoachondroplastic spondyloepiphyseal dysplasia syndrome">Pseudoachondroplastic spondyloepiphyseal dysplasia syndrome</a></span></li><li><span class="TLline"><a href="/medgen/60133" ref="tree=MeSH" title="MedGen record for Pseudoexfoliation glaucoma">Pseudoexfoliation glaucoma</a></span></li><li><span class="TLline"><a href="/medgen/10991" ref="tree=MeSH" title="MedGen record for Pseudohermaphroditism">Pseudohermaphroditism</a></span></li><li><span class="TLline"><a href="/medgen/18721" ref="tree=MeSH" title="MedGen record for Pseudohypoaldosteronism">Pseudohypoaldosteronism</a></span></li><li><span class="TLline"><a href="/medgen/488447" ref="tree=MeSH" title="MedGen record for Pseudohypoparathyroidism type I A">Pseudohypoparathyroidism type I A</a></span></li><li><span class="TLline"><a href="/medgen/18733" ref="tree=MeSH" title="MedGen record for Pseudoxanthoma elasticum">Pseudoxanthoma elasticum</a></span></li><li><span class="TLline"><a href="/medgen/18801" ref="tree=MeSH" title="MedGen record for Pyruvate carboxylase deficiency">Pyruvate carboxylase deficiency</a></span></li><li><span class="TLline"><a href="/medgen/19610" ref="tree=MeSH" title="MedGen record for Pyruvate dehydrogenase complex deficiency">Pyruvate dehydrogenase complex deficiency</a></span></li><li><span class="TLline"><a href="/medgen/61235" ref="tree=MeSH" title="MedGen record for Radial aplasia-thrombocytopenia syndrome">Radial aplasia-thrombocytopenia syndrome</a></span></li><li><span class="TLline"><a href="/medgen/45995" ref="tree=MeSH" title="MedGen record for Relapsing polychondritis">Relapsing polychondritis</a></span></li><li><span class="TLline"><a href="/medgen/90999" ref="tree=MeSH" title="MedGen record for Renal carnitine transport defect">Renal carnitine transport defect</a></span></li><li><span class="TLline"><a href="/medgen/56292" ref="tree=MeSH" title="MedGen record for Retinoschisis">Retinoschisis</a></span></li><li><span class="TLline"><a href="/medgen/48441" ref="tree=MeSH" title="MedGen record for Rett syndrome">Rett syndrome</a></span></li><li><span class="TLline"><a href="/medgen/887965" ref="tree=MeSH" title="MedGen record for Rhizomelic dysplasia">Rhizomelic dysplasia</a></span></li><li><span class="TLline"><a href="/medgen/371357" ref="tree=MeSH" title="MedGen record for Rippling muscle disease 2">Rippling muscle disease 2</a></span></li><li><span class="TLline"><a href="/medgen/95931" ref="tree=MeSH" title="MedGen record for Roberts-SC phocomelia syndrome">Roberts-SC phocomelia syndrome</a></span></li><li><span class="TLline"><a href="/medgen/78535" ref="tree=MeSH" title="MedGen record for Robinow syndrome">Robinow syndrome</a></span></li><li><span class="TLline"><a href="/medgen/104492" ref="tree=MeSH" title="MedGen record for Russell-Silver syndrome">Russell-Silver syndrome</a></span></li><li><span class="TLline"><a href="/medgen/120490" ref="tree=MeSH" title="MedGen record for SAPHO syndrome">SAPHO syndrome</a></span></li><li><span class="TLline"><a href="/medgen/3324" ref="tree=MeSH" title="MedGen record for Schilder disease">Schilder disease</a></span></li><li><span class="TLline"><a href="/medgen/164078" ref="tree=MeSH" title="MedGen record for Schimke immuno-osseous dysplasia">Schimke immuno-osseous dysplasia</a></span></li><li><span class="TLline"><a href="/medgen/120517" ref="tree=MeSH" title="MedGen record for Schinzel-Giedion syndrome">Schinzel-Giedion syndrome</a></span></li><li><span class="TLline"><a href="/medgen/20675" ref="tree=MeSH" title="MedGen record for Scimitar syndrome">Scimitar syndrome</a></span></li><li><span class="TLline"><a href="/medgen/11346" ref="tree=MeSH" title="MedGen record for Scleredema">Scleredema</a></span></li><li><span class="TLline"><a href="/medgen/120530" ref="tree=MeSH" title="MedGen record for Sclerosteosis">Sclerosteosis</a></span></li><li><span class="TLline"><a href="/medgen/19908" ref="tree=MeSH" title="MedGen record for Sea-blue histiocyte syndrome">Sea-blue histiocyte syndrome</a></span></li><li><span class="TLline"><a href="/medgen/78534" ref="tree=MeSH" title="MedGen record for Seckel syndrome">Seckel syndrome</a></span></li><li><span class="TLline"><a href="/medgen/443521" ref="tree=MeSH" title="MedGen record for Selective Antibody Deficiency with Normal Immunoglobulins">Selective Antibody Deficiency with Normal Immunoglobulins</a></span></li><li><span class="TLline"><a href="/medgen/90926" ref="tree=MeSH" title="MedGen record for Septo-optic dysplasia sequence">Septo-optic dysplasia sequence</a></span></li><li><span class="TLline"><a href="/medgen/11412" ref="tree=MeSH" title="MedGen record for Short rib-polydactyly syndrome">Short rib-polydactyly syndrome</a></span></li><li><span class="TLline"><a href="/medgen/856639" ref="tree=MeSH" title="MedGen record for Short Stature Homeobox Deficiency">Short Stature Homeobox Deficiency</a></span></li><li><span class="TLline"><a href="/medgen/231160" ref="tree=MeSH" title="MedGen record for Shprintzen-Goldberg syndrome">Shprintzen-Goldberg syndrome</a></span></li><li><span class="TLline"><a href="/medgen/87466" ref="tree=MeSH" title="MedGen record for Sitosterolemia">Sitosterolemia</a></span></li><li><span class="TLline"><a href="/medgen/7331" ref="tree=MeSH" title="MedGen record for Situs inversus with levocardia">Situs inversus with levocardia</a></span></li><li><span class="TLline"><a href="/medgen/11443" ref="tree=MeSH" title="MedGen record for Sjögren-Larsson syndrome">Sjögren-Larsson syndrome</a></span></li><li><span class="TLline"><a href="/medgen/61231" ref="tree=MeSH" title="MedGen record for Smith-Lemli-Opitz syndrome">Smith-Lemli-Opitz syndrome</a></span></li><li><span class="TLline"><a href="/medgen/162881" ref="tree=MeSH" title="MedGen record for Smith-Magenis syndrome">Smith-Magenis syndrome</a></span></li><li><span class="TLline"><a href="/medgen/61232" ref="tree=MeSH" title="MedGen record for Sotos syndrome">Sotos syndrome</a></span></li><li><span class="TLline"><a href="/medgen/101818" ref="tree=MeSH" title="MedGen record for Spasmodic torticollis">Spasmodic torticollis</a></span></li><li><span class="TLline"><a href="/medgen/7755" ref="tree=MeSH" title="MedGen record for Spinal muscular atrophy">Spinal muscular atrophy</a></span></li><li><span class="TLline"><a href="/medgen/266247" ref="tree=MeSH" title="MedGen record for Sponastrime dysplasia">Sponastrime dysplasia</a></span></li><li><span class="TLline"><a href="/medgen/350960" ref="tree=MeSH" title="MedGen record for Spondyloepimetaphyseal dysplasia with multiple dislocations">Spondyloepimetaphyseal dysplasia with multiple dislocations</a></span></li><li><span class="TLline"><a href="/medgen/163223" ref="tree=MeSH" title="MedGen record for Spondyloperipheral dysplasia">Spondyloperipheral dysplasia</a></span></li><li><span class="TLline"><a href="/medgen/75734" ref="tree=MeSH" title="MedGen record for Stargardt disease">Stargardt disease</a></span></li><li><span class="TLline"><a href="/medgen/863232" ref="tree=MeSH" title="MedGen record for STAT3-related early-onset multisystem autoimmune disease">STAT3-related early-onset multisystem autoimmune disease</a></span></li><li><span class="TLline"><a href="/medgen/11586" ref="tree=MeSH" title="MedGen record for Status epilepticus">Status epilepticus</a></span></li><li><span class="TLline"><a href="/medgen/120521" ref="tree=MeSH" title="MedGen record for Stickler syndrome">Stickler syndrome</a></span></li><li><span class="TLline"><a href="/medgen/348877" ref="tree=MeSH" title="MedGen record for Stiff skin syndrome">Stiff skin syndrome</a></span></li><li><span class="TLline"><a href="/medgen/39017" ref="tree=MeSH" title="MedGen record for Stiff-man syndrome">Stiff-man syndrome</a></span></li><li><span class="TLline"><a href="/medgen/52527" ref="tree=MeSH" title="MedGen record for Subacute sclerosing panencephalitis">Subacute sclerosing panencephalitis</a></span></li><li><span class="TLline"><a href="/medgen/224724" ref="tree=MeSH" title="MedGen record for SUNCT syndrome">SUNCT syndrome</a></span></li><li><span class="TLline"><a href="/medgen/21404" ref="tree=MeSH" title="MedGen record for Superior mesenteric artery syndrome">Superior mesenteric artery syndrome</a></span></li><li><span class="TLline"><a href="/medgen/476151" ref="tree=MeSH" title="MedGen record for Surfactant Protein Deficiency">Surfactant Protein Deficiency</a></span></li><li><span class="TLline"><a href="/medgen/78107" ref="tree=MeSH" title="MedGen record for Swyer James Syndrome">Swyer James Syndrome</a></span></li><li><span class="TLline"><a href="/medgen/96071" ref="tree=MeSH" title="MedGen record for Symmetrical dyschromatosis of extremities">Symmetrical dyschromatosis of extremities</a></span></li><li><span class="TLline"><a href="/medgen/437845" ref="tree=MeSH" title="MedGen record for Synpolydactyly">Synpolydactyly</a></span></li><li><span class="TLline"><a href="/medgen/21449" ref="tree=MeSH" title="MedGen record for Syringomyelia">Syringomyelia</a></span></li><li><span class="TLline"><a href="/medgen/366029" ref="tree=MeSH" title="MedGen record for Takotsubo cardiomyopathy">Takotsubo cardiomyopathy</a></span></li><li><span class="TLline"><a href="/medgen/52644" ref="tree=MeSH" title="MedGen record for Tangier disease">Tangier disease</a></span></li><li><span class="TLline"><a href="/medgen/11713" ref="tree=MeSH" title="MedGen record for Tay-Sachs disease">Tay-Sachs disease</a></span></li><li><span class="TLline"><a href="/medgen/12182" ref="tree=MeSH" title="MedGen record for Tear film insufficiency">Tear film insufficiency</a></span></li><li><span class="TLline"><a href="/medgen/21124" ref="tree=MeSH" title="MedGen record for Thanatophoric dysplasia">Thanatophoric dysplasia</a></span></li><li><span class="TLline"><a href="/medgen/21158" ref="tree=MeSH" title="MedGen record for Thoracic outlet syndrome">Thoracic outlet syndrome</a></span></li><li><span class="TLline"><a href="/medgen/349976" ref="tree=MeSH" title="MedGen record for Thrombocytopenia 2">Thrombocytopenia 2</a></span></li><li><span class="TLline"><a href="/medgen/289647" ref="tree=MeSH" title="MedGen record for Thyroid dysgenesis">Thyroid dysgenesis</a></span></li><li><span class="TLline"><a href="/medgen/424854" ref="tree=MeSH" title="MedGen record for Thyroid hormone resistance syndrome">Thyroid hormone resistance syndrome</a></span></li><li><span class="TLline"><a href="/medgen/1374188" ref="tree=MeSH" title="MedGen record for Tissue Kallikrein Deficiency">Tissue Kallikrein Deficiency</a></span></li><li><span class="TLline"><a href="/medgen/21575" ref="tree=MeSH" title="MedGen record for Togaviridae infectious disease">Togaviridae infectious disease</a></span></li><li><span class="TLline"><a href="/medgen/21197" ref="tree=MeSH" title="MedGen record for Tolosa-Hunt syndrome">Tolosa-Hunt syndrome</a></span></li><li><span class="TLline"><a href="/medgen/137976" ref="tree=MeSH" title="MedGen record for Transcobalamin II deficiency">Transcobalamin II deficiency</a></span></li><li><span class="TLline"><a href="/medgen/83275" ref="tree=MeSH" title="MedGen record for Transient global amnesia">Transient global amnesia</a></span></li><li><span class="TLline"><a href="/medgen/21245" ref="tree=MeSH" title="MedGen record for Transposition of the great arteries">Transposition of the great arteries</a></span></li><li><span class="TLline"><a href="/medgen/66078" ref="tree=MeSH" title="MedGen record for Treacher Collins syndrome">Treacher Collins syndrome</a></span></li><li><span class="TLline"><a href="/medgen/3238" ref="tree=MeSH" title="MedGen record for Triatrial heart">Triatrial heart</a></span></li><li><span class="TLline"><a href="/medgen/140929" ref="tree=MeSH" title="MedGen record for Trichorhinophalangeal dysplasia type I">Trichorhinophalangeal dysplasia type I</a></span></li><li><span class="TLline"><a href="/medgen/363064" ref="tree=MeSH" title="MedGen record for Trichothiodystrophy">Trichothiodystrophy</a></span></li><li><span class="TLline"><a href="/medgen/90711" ref="tree=MeSH" title="MedGen record for Triploidy">Triploidy</a></span></li><li><span class="TLline"><a href="/medgen/78595" ref="tree=MeSH" title="MedGen record for True hermaphroditism">True hermaphroditism</a></span></li><li><span class="TLline"><a href="/medgen/21725" ref="tree=MeSH" title="MedGen record for Tuberculosis of meninges">Tuberculosis of meninges</a></span></li><li><span class="TLline"><a href="/medgen/181871" ref="tree=MeSH" title="MedGen record for Uniparental disomy">Uniparental disomy</a></span></li><li><span class="TLline"><a href="/medgen/78754" ref="tree=MeSH" title="MedGen record for Usher syndrome">Usher syndrome</a></span></li><li><span class="TLline"><a href="/medgen/61233" ref="tree=MeSH" title="MedGen record for Van der Woude syndrome">Van der Woude syndrome</a></span></li><li><span class="TLline"><a href="/medgen/58118" ref="tree=MeSH" title="MedGen record for Variegate porphyria">Variegate porphyria</a></span></li><li><span class="TLline"><a href="/medgen/82753" ref="tree=MeSH" title="MedGen record for Vascular ectasia of gastric antrum">Vascular ectasia of gastric antrum</a></span></li><li><span class="TLline"><a href="/medgen/854382" ref="tree=MeSH" title="MedGen record for Very long chain acyl-CoA dehydrogenase deficiency">Very long chain acyl-CoA dehydrogenase deficiency</a></span></li><li><span class="TLline"><a href="/medgen/465273" ref="tree=MeSH" title="MedGen record for Visceral heterotaxy">Visceral heterotaxy</a></span></li><li><span class="TLline"><a href="/medgen/137920" ref="tree=MeSH" title="MedGen record for Vitelliform macular dystrophy">Vitelliform macular dystrophy</a></span></li><li><span class="TLline"><a href="/medgen/22599" ref="tree=MeSH" title="MedGen record for Vogt-Koyanagi-Harada disease">Vogt-Koyanagi-Harada disease</a></span></li><li><span class="TLline"><a href="/medgen/473809" ref="tree=MeSH" title="MedGen record for Waardenburg syndrome">Waardenburg syndrome</a></span></li><li><span class="TLline"><a href="/medgen/75782" ref="tree=MeSH" title="MedGen record for Wandering spleen">Wandering spleen</a></span></li><li><span class="TLline"><a href="/medgen/53065" ref="tree=MeSH" title="MedGen record for Waterhouse-Friderichsen Syndrome">Waterhouse-Friderichsen Syndrome</a></span></li><li><span class="TLline"><a href="/medgen/120511" ref="tree=MeSH" title="MedGen record for Weaver syndrome">Weaver syndrome</a></span></li><li><span class="TLline"><a href="/medgen/82705" ref="tree=MeSH" title="MedGen record for Weill-Marchesani syndrome">Weill-Marchesani syndrome</a></span></li><li><span class="TLline"><a href="/medgen/83883" ref="tree=MeSH" title="MedGen record for Wernicke-Korsakoff syndrome">Wernicke-Korsakoff syndrome</a></span></li><li><span class="TLline"><a href="/medgen/11519" ref="tree=MeSH" title="MedGen record for West syndrome">West syndrome</a></span></li><li><span class="TLline"><a href="/medgen/7347" ref="tree=MeSH" title="MedGen record for Whipple disease">Whipple disease</a></span></li><li><span class="TLline"><a href="/medgen/328433" ref="tree=MeSH" title="MedGen record for White sponge nevus">White sponge nevus</a></span></li><li><span class="TLline"><a href="/medgen/59799" ref="tree=MeSH" title="MedGen record for Williams syndrome">Williams syndrome</a></span></li><li><span class="TLline"><a href="/medgen/42426" ref="tree=MeSH" title="MedGen record for Wilson disease">Wilson disease</a></span></li><li><span class="TLline"><a href="/medgen/98152" ref="tree=MeSH" title="MedGen record for Winchester syndrome">Winchester syndrome</a></span></li><li><span class="TLline"><a href="/medgen/21923" ref="tree=MeSH" title="MedGen record for Wolfram syndrome">Wolfram syndrome</a></span></li><li><span class="TLline"><a href="/medgen/337334" ref="tree=MeSH" title="MedGen record for X-linked intellectual disability Cabezas type">X-linked intellectual disability Cabezas type</a></span></li><li><span class="TLline"><a href="/medgen/930080" ref="tree=MeSH" title="MedGen record for Xeroderma pigmentosum-Cockayne syndrome complex">Xeroderma pigmentosum-Cockayne syndrome complex</a></span></li><li><span class="TLline"><a href="/medgen/416028" ref="tree=MeSH" title="MedGen record for XXXY and XXXXY Syndrome">XXXY and XXXXY Syndrome</a></span></li><li><span class="TLline"><a href="/medgen/1786817" ref="tree=MeSH" title="MedGen record for YARSopathy">YARSopathy</a></span></li><li><span class="TLline"><a href="/medgen/113164" ref="tree=MeSH" title="MedGen record for Yellow nail syndrome">Yellow nail syndrome</a></span></li></ul></li></ul></li></ul></li></ul></li></ul></li></ul></li></ul></div></div></div></div>
|
||
</div>
|
||
|
||
<div class="portlet mgSection" id="ID_105">
|
||
<div class="portlet_head mgSectionHead ui-widget-header"><h1 class="nl" id="Professional_guidelines">Professional guidelines</h1><a sid="105" href="#" class="portlet_shutter" title="Show/hide content"></a></div>
|
||
<div class="portlet_content ln"><h3 class="subhead">PubMed<a class="help jig-ncbi-popper" data-jig="ncbipopper" href="#guidelinesHelpPM"><img class="pulldown" src="//static.pubmed.gov/portal/portal3rc.fcgi/4223267/img/4204968" /></a></h3>
|
||
<div class="nl"><a target="_blank" href="/pubmed/27418059">Pituitary stalk thickening: the role of an innovative MRI imaging analysis which may assist in determining clinical management.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Sbardella E,
|
||
Joseph RN,
|
||
Jafar-Mohammadi B,
|
||
Isidori AM,
|
||
Cudlip S,
|
||
Grossman AB</span><br />
|
||
<span class="medgenPMjournal">Eur J Endocrinol</span>
|
||
2016 Oct;175(4):255-63.
|
||
Epub 2016 Jul 14
|
||
doi: 10.1530/EJE-16-0455.
|
||
<span class="bold">PMID: </span><a href="/pubmed/27418059" target="_blank">27418059</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=(%22non-neoplastic%20disorder%22%5Btiab%3A~0%5D)%20AND%20(%22english%20and%20humans%22%5BFilter%5D)%20AND%20(%20(%22practice%20guideline%22%5BFilter%5D)%20OR%20(practice*%5Btitl%5D%20AND%20(guideline%5Btitl%5D%20OR%20parameter%5Btitl%5D%20OR%20resource%5Btitl%5D%20OR%20bulletin%5Btitl%5D%20OR%20best%5Btitl%5D))%20OR%20(genetic*%5Btitl%5D%20AND%20(evaluation%5Btitl%5D%20OR%20counseling%5Btitl%5D%20OR%20screening%5Btitl%5D%20OR%20test*%5Btitl%5D))%20OR%20(clinical%5Btitl%5D%20AND%20((expert%5Btitl%5D%20AND%20consensus%5Btitl%5D)%20OR%20utility%5Btitl%5D%20OR%20guideline*%5Btitl%5D))%20OR%20(management%5Btitl%5D%20AND%20(clinical%5Btitl%5D%20OR%20diagnos*%5Btitl%5D%20OR%20recommendation%5Btitl%5D%20OR%20pain%5Btitl%5D%20OR%20surveillance%5Btitl%5D%20OR%20emergency%5Btitl%5D%20OR%20guideline*%5Btitl%5D%20OR%20therap*))%20OR%20(treatment%5Btitl%5D%20AND%20((evaluation%5Btitl%5D%20AND%20diagnosis%5Btitl%5D)%20OR%20(assessment%5Btitl%5D%20AND%20prevention%5Btitl%5D)%20OR%20therap*))%20OR%20(Diagnos*%5Btitl%5D%20AND%20(prenatal%5Btitl%5D%20OR%20treatment%5Btitl%5D%20OR%20follow-up%5Btitl%5D%20OR%20statement%5Btitl%5D%20OR%20criteria%5Btitl%5D%20OR%20newborn%5Btitl%5D%20OR%20differential%5Btitl%5D%20OR%20neonatal%5Btitl%5D%20OR%20neonate%5Btitl%5D))%20OR%20(guideline*%5Btitl%5D%20AND%20(pharmacogenetic*%5Btitl%5D%20OR%20recommendation%5Btitl%5D%20OR%20therap*%5Btitl%5D%20OR%20evidence-based%5Btitl%5D%20OR%20consensus%5Btitl%5D%20OR%20(technical%5Btitl%5D%20AND%20standard*%5Btitl%5D)%20OR%20(molecular%5Btitl%5D%20AND%20testing%5Btitl%5D)))%20OR%20(risk%5Btitl%5D%20AND%20assessment%5Btitl%5D)%20OR%20(recommendation*%5Btitl%5D%20AND%20(statement%5Btitl%5D%20OR%20Evidence-based%5Btitl%5D%20OR%20Consensus%5Btitl%5D))%20OR%20(care%20AND%20((Patient%5Btitl%5D%20AND%20standard*%5Btitl%5D)%20OR%20primary%5Btitl%5D%20OR%20psychosocial%5Btitl%5D))%20OR%20(Health%5Btitl%5D%20AND%20supervision%5Btitl%5D)%20OR%20(statement%5Btitl%5D%20AND%20(policy%5Btitl%5D%20OR%20position%5Btitl%5D%20OR%20Consensus%5Btitl%5D))%20OR%20(pharmacogenetics%5Btitl%5D%20AND%20(Dosing%5Btitl%5D%20OR%20therap*%5Btitl%5D%20OR%20genotype*%5Btitl%5D%20OR%20drug*%5Btitl%5D))%20OR%20(Chemotherapy%5Btitl%5D%20AND%20decision*%5Btitl%5D)%20OR%20(screening%5Btitl%5D%20AND%20(newborn%5Btitl%5D%20OR%20neonat*%5Btitl%5D%20OR%20detection%5Btitl%5D%20OR%20diagnos*%5Btitl%5D))%20OR%20(criteria%5Btitl%5D%20OR%20genotype*%5Btitl%5D)%20)%20NOT%20(%22Case%20reports%22%5BPublication%20type%5D%20OR%20%22clinical%20study%22%5BPublication%20Type%5D%20OR%20%22randomized%20controlled%20trial%22%5BPublication%20Type%5D)" title="PubMed search">See all (1)</a></div></div>
|
||
</div>
|
||
<div class="display-none help-popup" id="guidelinesHelpPM">These guidelines are articles in PubMed that match specific search criteria developed by MedGen to capture the most relevant practice guidelines. This list may not be comprehensive and may include broader topics as well. See the <a href="/medgen/docs/faq/" title="Frequently asked questions" target="_blank">FAQ</a> for details.</div><div class="display-none help-popup" id="guidelinesHelpCurated">These guidelines are manually curated by the MedGen team
|
||
to supplement articles available in PubMed. See the <a href="/medgen/docs/faq/" title="Frequently asked questions" target="_blank">FAQ</a> for details.</div>
|
||
<div class="portlet mgSection" id="ID_103">
|
||
<div class="portlet_head mgSectionHead ui-widget-header"><h1 class="nl" id="Recent_clinical_studies">Recent clinical studies</h1><a sid="103" href="#" class="portlet_shutter" title="Show/hide content"></a></div>
|
||
<div class="portlet_content ln"><h3 class="subhead">Etiology</h3>
|
||
<div class="nl"><a target="_blank" href="/pubmed/37374301">Ovarian Leydig Cell Tumor and Ovarian Hyperthecosis in a Postmenopausal Woman: A Case Report and Literature Review.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Bužinskienė D,
|
||
Marčiukaitytė R,
|
||
Šidlovska E,
|
||
Rudaitis V</span><br />
|
||
<span class="medgenPMjournal">Medicina (Kaunas)</span>
|
||
2023 Jun 6;59(6)
|
||
doi: 10.3390/medicina59061097.
|
||
<span class="bold">PMID: </span><a href="/pubmed/37374301" target="_blank">37374301</a><a href="/pmc/articles/PMC10304025" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/27418059">Pituitary stalk thickening: the role of an innovative MRI imaging analysis which may assist in determining clinical management.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Sbardella E,
|
||
Joseph RN,
|
||
Jafar-Mohammadi B,
|
||
Isidori AM,
|
||
Cudlip S,
|
||
Grossman AB</span><br />
|
||
<span class="medgenPMjournal">Eur J Endocrinol</span>
|
||
2016 Oct;175(4):255-63.
|
||
Epub 2016 Jul 14
|
||
doi: 10.1530/EJE-16-0455.
|
||
<span class="bold">PMID: </span><a href="/pubmed/27418059" target="_blank">27418059</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/17256137">Analysis of the factors related to the decision of restoring intestinal continuity after Hartmann's procedure.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Roque-Castellano C,
|
||
Marchena-Gomez J,
|
||
Hemmersbach-Miller M,
|
||
Acosta-Merida A,
|
||
Rodriguez-Mendez A,
|
||
Fariña-Castro R,
|
||
Hernandez-Romero J</span><br />
|
||
<span class="medgenPMjournal">Int J Colorectal Dis</span>
|
||
2007 Sep;22(9):1091-6.
|
||
Epub 2007 Jan 26
|
||
doi: 10.1007/s00384-007-0272-4.
|
||
<span class="bold">PMID: </span><a href="/pubmed/17256137" target="_blank">17256137</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/7023312">Inappropriate secretion of thyroid-stimulating hormone.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMjournal">Ann Intern Med</span>
|
||
1981 Sep;95(3):339-51.
|
||
doi: 10.7326/0003-4819-95-3-339.
|
||
<span class="bold">PMID: </span><a href="/pubmed/7023312" target="_blank">7023312</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Non-Neoplastic%20Disorder%22%20AND%20Etiology%2Fbroad%5Bfilter%5D%20%20AND%20%22english%20and%20humans%22%5Bfilter%5D%20NOT%20comment%5BPTYP%5D%20NOT%20letter%5BPTYP%5D" title="PubMed search">See all (4)</a></div><h3 class="subhead">Diagnosis</h3>
|
||
<div class="nl"><a target="_blank" href="/pubmed/37374301">Ovarian Leydig Cell Tumor and Ovarian Hyperthecosis in a Postmenopausal Woman: A Case Report and Literature Review.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Bužinskienė D,
|
||
Marčiukaitytė R,
|
||
Šidlovska E,
|
||
Rudaitis V</span><br />
|
||
<span class="medgenPMjournal">Medicina (Kaunas)</span>
|
||
2023 Jun 6;59(6)
|
||
doi: 10.3390/medicina59061097.
|
||
<span class="bold">PMID: </span><a href="/pubmed/37374301" target="_blank">37374301</a><a href="/pmc/articles/PMC10304025" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/30829677">Sclerosing Mesenteritis.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Danford CJ,
|
||
Lin SC,
|
||
Wolf JL</span><br />
|
||
<span class="medgenPMjournal">Am J Gastroenterol</span>
|
||
2019 Jun;114(6):867-873.
|
||
doi: 10.14309/ajg.0000000000000167.
|
||
<span class="bold">PMID: </span><a href="/pubmed/30829677" target="_blank">30829677</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/27418059">Pituitary stalk thickening: the role of an innovative MRI imaging analysis which may assist in determining clinical management.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Sbardella E,
|
||
Joseph RN,
|
||
Jafar-Mohammadi B,
|
||
Isidori AM,
|
||
Cudlip S,
|
||
Grossman AB</span><br />
|
||
<span class="medgenPMjournal">Eur J Endocrinol</span>
|
||
2016 Oct;175(4):255-63.
|
||
Epub 2016 Jul 14
|
||
doi: 10.1530/EJE-16-0455.
|
||
<span class="bold">PMID: </span><a href="/pubmed/27418059" target="_blank">27418059</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/22795933">Balloon catheter sialoplasty: a safety and feasibility pilot study.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Sionis S,
|
||
Vedele A,
|
||
Brennan PA,
|
||
Fanni D,
|
||
Puxeddu R</span><br />
|
||
<span class="medgenPMjournal">Br J Oral Maxillofac Surg</span>
|
||
2013 Apr;51(3):228-30.
|
||
Epub 2012 Jul 15
|
||
doi: 10.1016/j.bjoms.2012.06.011.
|
||
<span class="bold">PMID: </span><a href="/pubmed/22795933" target="_blank">22795933</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/7560355">Massive papillary dermal fatty infiltration in a patient with psoriasis.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Lee J,
|
||
Bhawan J,
|
||
Rothman K</span><br />
|
||
<span class="medgenPMjournal">J Cutan Pathol</span>
|
||
1995 Apr;22(2):182-4.
|
||
doi: 10.1111/j.1600-0560.1995.tb01405.x.
|
||
<span class="bold">PMID: </span><a href="/pubmed/7560355" target="_blank">7560355</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Non-Neoplastic%20Disorder%22%20AND%20Diagnosis%2Fbroad%5Bfilter%5D%20%20AND%20%22english%20and%20humans%22%5Bfilter%5D%20NOT%20comment%5BPTYP%5D%20NOT%20letter%5BPTYP%5D" title="PubMed search">See all (9)</a></div><h3 class="subhead">Therapy</h3>
|
||
<div class="nl"><a target="_blank" href="/pubmed/30076806">Myositis Ossificans Traumatica of the Medial Pterygoid Muscle After Third Molar Tooth Extraction: A Case Report and Review of Literature.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Karaali S,
|
||
Emekli U</span><br />
|
||
<span class="medgenPMjournal">J Oral Maxillofac Surg</span>
|
||
2018 Nov;76(11):2284.e1-2284.e5.
|
||
Epub 2018 Jul 10
|
||
doi: 10.1016/j.joms.2018.06.174.
|
||
<span class="bold">PMID: </span><a href="/pubmed/30076806" target="_blank">30076806</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/17256137">Analysis of the factors related to the decision of restoring intestinal continuity after Hartmann's procedure.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Roque-Castellano C,
|
||
Marchena-Gomez J,
|
||
Hemmersbach-Miller M,
|
||
Acosta-Merida A,
|
||
Rodriguez-Mendez A,
|
||
Fariña-Castro R,
|
||
Hernandez-Romero J</span><br />
|
||
<span class="medgenPMjournal">Int J Colorectal Dis</span>
|
||
2007 Sep;22(9):1091-6.
|
||
Epub 2007 Jan 26
|
||
doi: 10.1007/s00384-007-0272-4.
|
||
<span class="bold">PMID: </span><a href="/pubmed/17256137" target="_blank">17256137</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/7199614">Chronic idiopathic thrombocytopenic purpura (ITP:) development of acute non-lymphocytic leukemia subsequent to treatment with cyclophosphamide.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Krause JR</span><br />
|
||
<span class="medgenPMjournal">Med Pediatr Oncol</span>
|
||
1982;10(1):61-5.
|
||
doi: 10.1002/mpo.2950100110.
|
||
<span class="bold">PMID: </span><a href="/pubmed/7199614" target="_blank">7199614</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/7023312">Inappropriate secretion of thyroid-stimulating hormone.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMjournal">Ann Intern Med</span>
|
||
1981 Sep;95(3):339-51.
|
||
doi: 10.7326/0003-4819-95-3-339.
|
||
<span class="bold">PMID: </span><a href="/pubmed/7023312" target="_blank">7023312</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/445330">Therapy-related leukemia: a panmyelosis.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Foucar K,
|
||
McKenna RW,
|
||
Bloomfield CD,
|
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Bowers TK,
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Brunning RD</span><br />
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1979 Apr;43(4):1285-96.
|
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doi: 10.1002/1097-0142(197904)43:4<1285::aid-cncr2820430416>3.0.co;2-j.
|
||
<span class="bold">PMID: </span><a href="/pubmed/445330" target="_blank">445330</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Non-Neoplastic%20Disorder%22%20AND%20Therapy%2Fbroad%5Bfilter%5D%20%20AND%20%22english%20and%20humans%22%5Bfilter%5D%20NOT%20comment%5BPTYP%5D%20NOT%20letter%5BPTYP%5D" title="PubMed search">See all (5)</a></div><h3 class="subhead">Prognosis</h3>
|
||
<div class="nl"><a target="_blank" href="/pubmed/37374301">Ovarian Leydig Cell Tumor and Ovarian Hyperthecosis in a Postmenopausal Woman: A Case Report and Literature Review.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Bužinskienė D,
|
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Marčiukaitytė R,
|
||
Šidlovska E,
|
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Rudaitis V</span><br />
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<span class="medgenPMjournal">Medicina (Kaunas)</span>
|
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2023 Jun 6;59(6)
|
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doi: 10.3390/medicina59061097.
|
||
<span class="bold">PMID: </span><a href="/pubmed/37374301" target="_blank">37374301</a><a href="/pmc/articles/PMC10304025" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/30829677">Sclerosing Mesenteritis.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Danford CJ,
|
||
Lin SC,
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Wolf JL</span><br />
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<span class="medgenPMjournal">Am J Gastroenterol</span>
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2019 Jun;114(6):867-873.
|
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doi: 10.14309/ajg.0000000000000167.
|
||
<span class="bold">PMID: </span><a href="/pubmed/30829677" target="_blank">30829677</a></div>
|
||
|
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<div class="nl"><a target="_blank" href="/pubmed/27418059">Pituitary stalk thickening: the role of an innovative MRI imaging analysis which may assist in determining clinical management.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Sbardella E,
|
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Joseph RN,
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||
Jafar-Mohammadi B,
|
||
Isidori AM,
|
||
Cudlip S,
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Grossman AB</span><br />
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<span class="medgenPMjournal">Eur J Endocrinol</span>
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2016 Oct;175(4):255-63.
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Epub 2016 Jul 14
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doi: 10.1530/EJE-16-0455.
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<span class="bold">PMID: </span><a href="/pubmed/27418059" target="_blank">27418059</a></div>
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||
<div class="nl"><a target="_blank" href="/pubmed/17256137">Analysis of the factors related to the decision of restoring intestinal continuity after Hartmann's procedure.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Roque-Castellano C,
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Marchena-Gomez J,
|
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Hemmersbach-Miller M,
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Acosta-Merida A,
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Rodriguez-Mendez A,
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Fariña-Castro R,
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Hernandez-Romero J</span><br />
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<span class="medgenPMjournal">Int J Colorectal Dis</span>
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2007 Sep;22(9):1091-6.
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Epub 2007 Jan 26
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doi: 10.1007/s00384-007-0272-4.
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<span class="bold">PMID: </span><a href="/pubmed/17256137" target="_blank">17256137</a></div>
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|
||
<div class="nl"><a target="_blank" href="/pubmed/7199614">Chronic idiopathic thrombocytopenic purpura (ITP:) development of acute non-lymphocytic leukemia subsequent to treatment with cyclophosphamide.</a></div>
|
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<div class="portlet_content ln"><span class="medgenPMauthor">Krause JR</span><br />
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<span class="medgenPMjournal">Med Pediatr Oncol</span>
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doi: 10.1002/mpo.2950100110.
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<span class="bold">PMID: </span><a href="/pubmed/7199614" target="_blank">7199614</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Non-Neoplastic%20Disorder%22%20AND%20Prognosis%2Fbroad%5Bfilter%5D%20%20AND%20%22english%20and%20humans%22%5Bfilter%5D%20NOT%20comment%5BPTYP%5D%20NOT%20letter%5BPTYP%5D" title="PubMed search">See all (5)</a></div><h3 class="subhead">Clinical prediction guides</h3>
|
||
<div class="nl"><a target="_blank" href="/pubmed/27418059">Pituitary stalk thickening: the role of an innovative MRI imaging analysis which may assist in determining clinical management.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Sbardella E,
|
||
Joseph RN,
|
||
Jafar-Mohammadi B,
|
||
Isidori AM,
|
||
Cudlip S,
|
||
Grossman AB</span><br />
|
||
<span class="medgenPMjournal">Eur J Endocrinol</span>
|
||
2016 Oct;175(4):255-63.
|
||
Epub 2016 Jul 14
|
||
doi: 10.1530/EJE-16-0455.
|
||
<span class="bold">PMID: </span><a href="/pubmed/27418059" target="_blank">27418059</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/17845151">Cranial fasciitis in an 8-year-old boy: clinical and histopathologic features.</a></div>
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||
<div class="portlet_content ln"><span class="medgenPMauthor">Yébenes M,
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Gilaberte M,
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Romaní J,
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Lloreta J,
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Pujol RM</span><br />
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<span class="medgenPMjournal">Pediatr Dermatol</span>
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2007 Jul-Aug;24(4):E26-30.
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doi: 10.1111/j.1525-1470.2007.00434.x.
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<span class="bold">PMID: </span><a href="/pubmed/17845151" target="_blank">17845151</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/17256137">Analysis of the factors related to the decision of restoring intestinal continuity after Hartmann's procedure.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Roque-Castellano C,
|
||
Marchena-Gomez J,
|
||
Hemmersbach-Miller M,
|
||
Acosta-Merida A,
|
||
Rodriguez-Mendez A,
|
||
Fariña-Castro R,
|
||
Hernandez-Romero J</span><br />
|
||
<span class="medgenPMjournal">Int J Colorectal Dis</span>
|
||
2007 Sep;22(9):1091-6.
|
||
Epub 2007 Jan 26
|
||
doi: 10.1007/s00384-007-0272-4.
|
||
<span class="bold">PMID: </span><a href="/pubmed/17256137" target="_blank">17256137</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/7560355">Massive papillary dermal fatty infiltration in a patient with psoriasis.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Lee J,
|
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Bhawan J,
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Rothman K</span><br />
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<span class="medgenPMjournal">J Cutan Pathol</span>
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1995 Apr;22(2):182-4.
|
||
doi: 10.1111/j.1600-0560.1995.tb01405.x.
|
||
<span class="bold">PMID: </span><a href="/pubmed/7560355" target="_blank">7560355</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Non-Neoplastic%20Disorder%22%20AND%20Clinical%20prediction%20guides%2Fbroad%5Bfilter%5D%20%20AND%20%22english%20and%20humans%22%5Bfilter%5D%20NOT%20comment%5BPTYP%5D%20NOT%20letter%5BPTYP%5D" title="PubMed search">See all (4)</a></div></div>
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