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<!--
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UID=508816
|
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ConceptID=C0151746
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-->
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<!--imgCountBooks = 0--><h1 class="medgenTitle"><div class="MedGenTitleText">Abnormal renal physiology</div></h1><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>508816</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.">C0151746</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Pathologic Function</dd></dl></div></div><table class="medgenTable"><tbody><tr><td>Synonym:</td>
|
||
<td>Kidney dysfunction</td></tr>
|
||
<tr><td><span class="bold">SNOMED CT: </span></td>
|
||
<td>Abnormal renal function (39539005)</td></tr>
|
||
<tr><td colspan="2" class="small"> </td></tr><tr><td>HPO:</td>
|
||
<td><a target="_blank" title="Human Phenotype Ontology" href="https://hpo.jax.org/app/browse/term/HP:0012211">HP:0012211</a></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>
|
||
<div class="portlet_content ln">An abnormal functionality of the kidney. [from <a title="Human Phenotype Ontology" href="http://www.human-phenotype-ontology.org" class="defSource" target="_blank">HPO</a>]</div>
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<div class="portlet mgSection" id="ID_118">
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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 Ccolor round" title="Clinical test"><a target="_blank" href="/gtr/tests/?term=C0151746[DISCUI]&test_type=Clinical&redirect=true" ref="ncbi_uid=508816">C</a></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">Abnormal renal physiology</span></li></ul></div></div></div></div></div><div id="tabMGEN"><div class="ds_tree"><ul><li><span class="TLline"><a href="/medgen/871309" ref="tree=MeSH" title="MedGen record for Abnormality of prenatal development or birth">Abnormality of prenatal development or birth</a></span><ul><li><span class="TLline"><a href="/medgen/1254" ref="tree=MeSH" title="MedGen record for Fetal anomaly">Fetal anomaly</a></span><ul><li><span class="TLline"><a href="/medgen/474891" ref="tree=MeSH" title="MedGen record for Congenital Systemic Disorder">Congenital Systemic Disorder</a></span><ul><li><span class="TLline"><a href="/medgen/52948" ref="tree=MeSH" title="MedGen record for Abnormality of the genitourinary system">Abnormality of the genitourinary system</a></span><ul><li><span class="TLline"><a href="/medgen/867444" ref="tree=MeSH" title="MedGen record for Abnormality of the urinary system">Abnormality of the urinary system</a></span><ul><li><span class="TLline"><a href="/medgen/869020" ref="tree=MeSH" title="MedGen record for Abnormality of the urinary system physiology">Abnormality of the urinary system physiology</a></span><ul><li><span class="matched_ds">Abnormal renal physiology</span><ul><li><span class="TLline"><a href="/medgen/489765" ref="tree=MeSH" title="MedGen record for Abnormal glomerular filtration rate">Abnormal glomerular filtration rate</a></span><ul><li><span class="TLline"><a href="/medgen/163428" ref="tree=MeSH" title="MedGen record for Decreased glomerular filtration rate">Decreased glomerular filtration rate</a></span></li><li><span class="TLline"><a href="/medgen/489766" ref="tree=MeSH" title="MedGen record for Increased glomerular filtration rate">Increased glomerular filtration rate</a></span></li></ul></li><li><span class="TLline"><a href="/medgen/869159" ref="tree=MeSH" title="MedGen record for Abnormality of renal excretion">Abnormality of renal excretion</a></span><ul><li><span class="TLline"><a href="/medgen/786049" ref="tree=MeSH" title="MedGen record for Abnormal urine output">Abnormal urine output</a></span><ul><li><span class="TLline"><a href="/medgen/854570" ref="tree=MeSH" title="MedGen record for Decreased urine output">Decreased urine output</a></span></li><li><span class="TLline"><a href="/medgen/19404" ref="tree=MeSH" title="MedGen record for Polyuria">Polyuria</a></span></li></ul></li><li><span class="TLline"><a href="/medgen/409704" ref="tree=MeSH" title="MedGen record for Decreased renal tubular phosphate excretion">Decreased renal tubular phosphate excretion</a></span></li><li><span class="TLline"><a href="/medgen/1864191" ref="tree=MeSH" title="MedGen record for Elevated fractional excretion of urate">Elevated fractional excretion of urate</a></span></li><li><span class="TLline"><a href="/medgen/409813" ref="tree=MeSH" title="MedGen record for Impaired renal uric acid clearance">Impaired renal uric acid clearance</a></span></li></ul></li><li><span class="TLline"><a href="/medgen/869319" ref="tree=MeSH" title="MedGen record for Elevated alkaline phosphatase of renal origin">Elevated alkaline phosphatase of renal origin</a></span></li><li><span class="TLline"><a href="/medgen/42403" ref="tree=MeSH" title="MedGen record for Hemolytic-uremic syndrome">Hemolytic-uremic syndrome</a></span><ul><li><span class="TLline"><a href="/medgen/444141" ref="tree=MeSH" title="MedGen record for Atypical hemolytic-uremic syndrome">Atypical hemolytic-uremic syndrome</a></span><ul><li><span class="TLline"><a href="/medgen/1842625" ref="tree=MeSH" title="MedGen record for Atypical hemolytic uremic syndrome with complement gene abnormality">Atypical hemolytic uremic syndrome with complement gene abnormality</a></span></li><li><span class="TLline"><a href="/medgen/1788163" ref="tree=MeSH" title="MedGen record for Atypical Hemolytic Uremic Syndrome-4">Atypical Hemolytic Uremic Syndrome-4</a></span></li><li><span class="TLline"><a href="/medgen/1825998" ref="tree=MeSH" title="MedGen record for Atypical hemolytic-uremic syndrome with anti-factor H antibodies">Atypical hemolytic-uremic syndrome with anti-factor H antibodies</a></span></li><li><span class="TLline"><a href="/medgen/416691" ref="tree=MeSH" title="MedGen record for Atypical hemolytic-uremic syndrome with B factor anomaly">Atypical hemolytic-uremic syndrome with B factor anomaly</a></span></li><li><span class="TLline"><a href="/medgen/442875" ref="tree=MeSH" title="MedGen record for Atypical hemolytic-uremic syndrome with C3 anomaly">Atypical hemolytic-uremic syndrome with C3 anomaly</a></span></li><li><span class="TLline"><a href="/medgen/414542" ref="tree=MeSH" title="MedGen record for Atypical hemolytic-uremic syndrome with I factor anomaly">Atypical hemolytic-uremic syndrome with I factor anomaly</a></span></li><li><span class="TLline"><a href="/medgen/414167" ref="tree=MeSH" title="MedGen record for Atypical hemolytic-uremic syndrome with MCP/CD46 anomaly">Atypical hemolytic-uremic syndrome with MCP/CD46 anomaly</a></span></li><li><span class="TLline"><a href="/medgen/414541" ref="tree=MeSH" title="MedGen record for Atypical hemolytic-uremic syndrome with thrombomodulin anomaly">Atypical hemolytic-uremic syndrome with thrombomodulin anomaly</a></span></li><li><span class="TLline"><a href="/medgen/885565" ref="tree=MeSH" title="MedGen record for Familial Atypical Hemolytic-Uremic Syndrome">Familial Atypical Hemolytic-Uremic Syndrome</a></span></li><li><span class="TLline"><a href="/medgen/430731" ref="tree=MeSH" title="MedGen record for Hemolytic uremic syndrome, atypical, childhood">Hemolytic uremic syndrome, atypical, childhood</a></span></li><li><span class="TLline"><a href="/medgen/370773" ref="tree=MeSH" title="MedGen record for Hemolytic uremic syndrome, atypical, susceptibility to">Hemolytic uremic syndrome, atypical, susceptibility to</a></span></li><li><span class="TLline"><a href="/medgen/412743" ref="tree=MeSH" title="MedGen record for Hemolytic uremic syndrome, atypical, susceptibility to, 1">Hemolytic uremic syndrome, atypical, susceptibility to, 1</a></span></li></ul></li><li><span class="TLline"><a href="/medgen/1826167" ref="tree=MeSH" title="MedGen record for Atypical hemolytic-uremic syndrome with DGKE deficiency">Atypical hemolytic-uremic syndrome with DGKE deficiency</a></span></li><li><span class="TLline"><a href="/medgen/341256" ref="tree=MeSH" title="MedGen record for Cobalamin C disease">Cobalamin C disease</a></span></li><li><span class="TLline"><a href="/medgen/449003" ref="tree=MeSH" title="MedGen record for D-plus hemolytic uremic syndrome (D+HUS)">D-plus hemolytic uremic syndrome (D+HUS)</a></span></li><li><span class="TLline"><a href="/medgen/692756" ref="tree=MeSH" title="MedGen record for Diarrhea-associated hemolytic uremic syndrome">Diarrhea-associated hemolytic uremic syndrome</a></span></li><li><span class="TLline"><a href="/medgen/692757" ref="tree=MeSH" title="MedGen record for Diarrhea-negative hemolytic uremic syndrome">Diarrhea-negative hemolytic uremic syndrome</a></span></li><li><span class="TLline"><a href="/medgen/1826072" ref="tree=MeSH" title="MedGen record for Infection-related hemolytic uremic syndrome">Infection-related hemolytic uremic syndrome</a></span><ul><li><span class="TLline"><a href="/medgen/383843" ref="tree=MeSH" title="MedGen record for Shiga toxin-associated hemolytic uremic syndrome">Shiga toxin-associated hemolytic uremic syndrome</a></span></li><li><span class="TLline"><a href="/medgen/1842720" ref="tree=MeSH" title="MedGen record for Streptococcus pneumoniae-associated hemolytic uremic syndrome">Streptococcus pneumoniae-associated hemolytic uremic syndrome</a></span></li></ul></li></ul></li><li><span class="TLline"><a href="/medgen/1378965" ref="tree=MeSH" title="MedGen record for Impaired urinary acidification">Impaired urinary acidification</a></span></li><li><span class="TLline"><a href="/medgen/868273" ref="tree=MeSH" title="MedGen record for Isothenuria">Isothenuria</a></span></li><li><span class="TLline"><a href="/medgen/9635" ref="tree=MeSH" title="MedGen record for Kidney disorder">Kidney disorder</a></span><ul><li><span class="TLline"><a href="/medgen/658582" ref="tree=MeSH" title="MedGen record for Acquired calyceal diverticulum">Acquired calyceal diverticulum</a></span></li><li><span class="TLline"><a href="/medgen/888926" ref="tree=MeSH" title="MedGen record for Acute Uric Acid Nephropathy">Acute Uric Acid Nephropathy</a></span></li><li><span class="TLline"><a href="/medgen/358" ref="tree=MeSH" title="MedGen record for Anuria">Anuria</a></span></li><li><span class="TLline"><a href="/medgen/886404" ref="tree=MeSH" title="MedGen record for Aristolochic acid nephropathy">Aristolochic acid nephropathy</a></span></li><li><span class="TLline"><a href="/medgen/231917" ref="tree=MeSH" title="MedGen record for Bone Marrow Transplantation Nephropathy">Bone Marrow Transplantation Nephropathy</a></span></li><li><span class="TLline"><a href="/medgen/417699" ref="tree=MeSH" title="MedGen record for Childhood Kidney Disorder">Childhood Kidney Disorder</a></span></li><li><span class="TLline"><a href="/medgen/541466" ref="tree=MeSH" title="MedGen record for Chronic gouty nephropathy">Chronic gouty nephropathy</a></span></li><li><span class="TLline"><a href="/medgen/885556" ref="tree=MeSH" title="MedGen record for Chronic kidney disease mineral and bone disorder">Chronic kidney disease mineral and bone disorder</a></span></li><li><span class="TLline"><a href="/medgen/352142" ref="tree=MeSH" title="MedGen record for Cystic Kidney Disease">Cystic Kidney Disease</a></span><ul><li><span class="TLline"><a href="/medgen/852741" ref="tree=MeSH" title="MedGen record for Complex renal cyst">Complex renal cyst</a></span></li><li><span class="TLline"><a href="/medgen/881357" ref="tree=MeSH" title="MedGen record for Medullary Cystic Kidney Disease Type I">Medullary Cystic Kidney Disease Type I</a></span></li><li><span class="TLline"><a href="/medgen/882383" ref="tree=MeSH" title="MedGen record for Medullary Cystic Kidney Disease Type II">Medullary Cystic Kidney Disease Type II</a></span></li><li><span class="TLline"><a href="/medgen/5970" ref="tree=MeSH" title="MedGen record for Medullary sponge kidney">Medullary sponge kidney</a></span></li><li><span class="TLline"><a href="/medgen/811388" ref="tree=MeSH" title="MedGen record for Multicystic kidney dysplasia">Multicystic kidney dysplasia</a></span></li><li><span class="TLline"><a href="/medgen/9639" ref="tree=MeSH" title="MedGen record for Polycystic kidney disease">Polycystic kidney disease</a></span></li><li><span class="TLline"><a href="/medgen/78701" ref="tree=MeSH" title="MedGen record for Simple renal cyst">Simple renal cyst</a></span></li></ul></li><li><span class="TLline"><a href="/medgen/8349" ref="tree=MeSH" title="MedGen record for Diabetes insipidus">Diabetes insipidus</a></span><ul><li><span class="TLline"><a href="/medgen/1373297" ref="tree=MeSH" title="MedGen record for Adipsic Diabetes Insipidus">Adipsic Diabetes Insipidus</a></span></li><li><span class="TLline"><a href="/medgen/146919" ref="tree=MeSH" title="MedGen record for Central diabetes insipidus">Central diabetes insipidus</a></span></li><li><span class="TLline"><a href="/medgen/82829" ref="tree=MeSH" title="MedGen record for Dipsogenic diabetes insipidus">Dipsogenic diabetes insipidus</a></span></li><li><span class="TLline"><a href="/medgen/57876" ref="tree=MeSH" title="MedGen record for Nephrogenic diabetes insipidus">Nephrogenic diabetes insipidus</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></ul></li><li><span class="TLline"><a href="/medgen/8352" ref="tree=MeSH" title="MedGen record for Diabetic kidney disease">Diabetic kidney disease</a></span></li><li><span class="TLline"><a href="/medgen/853268" ref="tree=MeSH" title="MedGen record for Drug-Induced Nephropathy">Drug-Induced Nephropathy</a></span><ul><li><span class="TLline"><a href="/medgen/882402" ref="tree=MeSH" title="MedGen record for Antimicrobial - Induced Nephropathy">Antimicrobial - Induced Nephropathy</a></span></li><li><span class="TLline"><a href="/medgen/883247" ref="tree=MeSH" title="MedGen record for Bisphosphonate - Induced Nephropathy">Bisphosphonate - Induced Nephropathy</a></span></li><li><span class="TLline"><a href="/medgen/883866" ref="tree=MeSH" title="MedGen record for Calcineurin Inhibitor - Induced Nephropathy">Calcineurin Inhibitor - Induced Nephropathy</a></span></li><li><span class="TLline"><a href="/medgen/859325" ref="tree=MeSH" title="MedGen record for Calcineurin Nephrotoxicity">Calcineurin Nephrotoxicity</a></span></li><li><span class="TLline"><a href="/medgen/886988" ref="tree=MeSH" title="MedGen record for Chemotherapeutic Drug - Induced Nephropathy">Chemotherapeutic Drug - Induced Nephropathy</a></span></li><li><span class="TLline"><a href="/medgen/890119" ref="tree=MeSH" title="MedGen record for Contrast - Induced Nephropathy">Contrast - Induced Nephropathy</a></span></li><li><span class="TLline"><a href="/medgen/888846" ref="tree=MeSH" title="MedGen record for Lithium - Induced Nephropathy">Lithium - Induced Nephropathy</a></span></li><li><span class="TLline"><a href="/medgen/889680" ref="tree=MeSH" title="MedGen record for mTOR Inhibitor - Induced Nephropathy">mTOR Inhibitor - Induced Nephropathy</a></span></li><li><span class="TLline"><a href="/medgen/891267" ref="tree=MeSH" title="MedGen record for Nephropathy due to Aminoglycosides">Nephropathy due to Aminoglycosides</a></span></li><li><span class="TLline"><a href="/medgen/885611" ref="tree=MeSH" title="MedGen record for Nephropathy due to Amphotericin">Nephropathy due to Amphotericin</a></span></li><li><span class="TLline"><a href="/medgen/889597" ref="tree=MeSH" title="MedGen record for Nephropathy due to Analgesic Drugs">Nephropathy due to Analgesic Drugs</a></span></li><li><span class="TLline"><a href="/medgen/890603" ref="tree=MeSH" title="MedGen record for Nephropathy due to Ciclosporin">Nephropathy due to Ciclosporin</a></span></li><li><span class="TLline"><a href="/medgen/881442" ref="tree=MeSH" title="MedGen record for Nephropathy due to Cisplatin">Nephropathy due to Cisplatin</a></span></li><li><span class="TLline"><a href="/medgen/888463" ref="tree=MeSH" title="MedGen record for Nephropathy due to Tacrolimus">Nephropathy due to Tacrolimus</a></span></li><li><span class="TLline"><a href="/medgen/883346" ref="tree=MeSH" title="MedGen record for NSAID-Induced Nephropathy">NSAID-Induced Nephropathy</a></span></li></ul></li><li><span class="TLline"><a href="/medgen/4904" ref="tree=MeSH" title="MedGen record for Focal segmental glomerulosclerosis">Focal segmental glomerulosclerosis</a></span><ul><li><span class="TLline"><a href="/medgen/98337" ref="tree=MeSH" title="MedGen record for Chronic rejection of renal transplant">Chronic rejection of renal transplant</a></span></li><li><span class="TLline"><a href="/medgen/891201" ref="tree=MeSH" title="MedGen record for Focal Segmental Glomerulosclerosis Cellular Variant">Focal Segmental Glomerulosclerosis Cellular Variant</a></span></li><li><span class="TLline"><a href="/medgen/889144" ref="tree=MeSH" title="MedGen record for Focal Segmental Glomerulosclerosis Collapsing Variant">Focal Segmental Glomerulosclerosis Collapsing Variant</a></span></li><li><span class="TLline"><a href="/medgen/889682" ref="tree=MeSH" title="MedGen record for Focal Segmental Glomerulosclerosis Perihilar Variant">Focal Segmental Glomerulosclerosis Perihilar Variant</a></span></li><li><span class="TLline"><a href="/medgen/885369" ref="tree=MeSH" title="MedGen record for Focal Segmental Glomerulosclerosis Tip Lesion Variant">Focal Segmental Glomerulosclerosis Tip Lesion Variant</a></span></li><li><span class="TLline"><a href="/medgen/887152" ref="tree=MeSH" title="MedGen record for Focal Segmental Glomerulosclerosis, Not Otherwise Specified">Focal Segmental Glomerulosclerosis, Not Otherwise Specified</a></span></li><li><span class="TLline"><a href="/medgen/37145" ref="tree=MeSH" title="MedGen record for HIV-associated nephropathy">HIV-associated nephropathy</a></span></li><li><span class="TLline"><a href="/medgen/1008296" ref="tree=MeSH" title="MedGen record for Inherited focal segmental glomerulosclerosis">Inherited focal segmental glomerulosclerosis</a></span></li><li><span class="TLline"><a href="/medgen/884256" ref="tree=MeSH" title="MedGen record for Obesity Related Glomerulopathy">Obesity Related Glomerulopathy</a></span></li><li><span class="TLline"><a href="/medgen/313617" ref="tree=MeSH" title="MedGen record for Primary focal segmental glomerulosclerosis">Primary focal segmental glomerulosclerosis</a></span></li><li><span class="TLline"><a href="/medgen/354165" ref="tree=MeSH" title="MedGen record for Secondary Focal Segmental Glomerulosclerosis">Secondary Focal Segmental Glomerulosclerosis</a></span></li></ul></li><li><span class="TLline"><a href="/medgen/61248" ref="tree=MeSH" title="MedGen record for Glomerular sclerosis">Glomerular sclerosis</a></span><ul><li><span class="TLline"><a href="/medgen/355432" ref="tree=MeSH" title="MedGen record for Global glomerulosclerosis">Global glomerulosclerosis</a></span></li><li><span class="TLline"><a href="/medgen/83080" ref="tree=MeSH" title="MedGen record for Segmental glomerulosclerosis">Segmental glomerulosclerosis</a></span></li></ul></li><li><span class="TLline"><a href="/medgen/451033" ref="tree=MeSH" title="MedGen record for Glomerulopathy">Glomerulopathy</a></span><ul><li><span class="TLline"><a href="/medgen/412719" ref="tree=MeSH" title="MedGen record for Collapsing Glomerulopathy">Collapsing Glomerulopathy</a></span></li><li><span class="TLline"><a href="/medgen/866466" ref="tree=MeSH" title="MedGen record for Glomerulocystic Disease">Glomerulocystic Disease</a></span></li><li><span class="TLline"><a href="/medgen/868212" ref="tree=MeSH" title="MedGen record for Glomerulomegaly">Glomerulomegaly</a></span></li><li><span class="TLline"><a href="/medgen/926453" ref="tree=MeSH" title="MedGen record for Idiopathic Membranous Glomerulopathy">Idiopathic Membranous Glomerulopathy</a></span></li><li><span class="TLline"><a href="/medgen/926295" ref="tree=MeSH" title="MedGen record for Membranous Nephropathy - Secondary">Membranous Nephropathy - Secondary</a></span></li><li><span class="TLline"><a href="/medgen/885805" ref="tree=MeSH" title="MedGen record for Primary Collapsing Glomerulopathy">Primary Collapsing Glomerulopathy</a></span></li><li><span class="TLline"><a href="/medgen/890369" ref="tree=MeSH" title="MedGen record for Secondary Collapsing Glomerulopathy">Secondary Collapsing Glomerulopathy</a></span></li><li><span class="TLline"><a href="/medgen/886189" ref="tree=MeSH" title="MedGen record for Tip Lesion Glomerulopathy">Tip Lesion Glomerulopathy</a></span></li></ul></li><li><span class="TLline"><a href="/medgen/889431" ref="tree=MeSH" title="MedGen record for Hantavirus Nephropathy">Hantavirus Nephropathy</a></span></li><li><span class="TLline"><a href="/medgen/9224" ref="tree=MeSH" title="MedGen record for Hepatorenal syndrome">Hepatorenal syndrome</a></span></li><li><span class="TLline"><a href="/medgen/42531" ref="tree=MeSH" title="MedGen record for Hydronephrosis">Hydronephrosis</a></span><ul><li><span class="TLline"><a href="/medgen/885797" ref="tree=MeSH" title="MedGen record for Antenatal Hydronephrosis">Antenatal Hydronephrosis</a></span></li><li><span class="TLline"><a href="/medgen/78594" ref="tree=MeSH" title="MedGen record for Congenital hydronephrosis">Congenital hydronephrosis</a></span></li><li><span class="TLline"><a href="/medgen/889820" ref="tree=MeSH" title="MedGen record for P1 Hydronephrosis">P1 Hydronephrosis</a></span></li><li><span class="TLline"><a href="/medgen/887766" ref="tree=MeSH" title="MedGen record for P2 Hydronephrosis">P2 Hydronephrosis</a></span></li><li><span class="TLline"><a href="/medgen/887656" ref="tree=MeSH" title="MedGen record for P3 Hydronephrosis">P3 Hydronephrosis</a></span></li><li><span class="TLline"><a href="/medgen/11051" ref="tree=MeSH" title="MedGen record for Pyonephrosis">Pyonephrosis</a></span></li></ul></li><li><span class="TLline"><a href="/medgen/43782" ref="tree=MeSH" title="MedGen record for Hyperoxaluria">Hyperoxaluria</a></span><ul><li><span class="TLline"><a href="/medgen/5697" ref="tree=MeSH" title="MedGen record for Primary hyperoxaluria">Primary hyperoxaluria</a></span></li></ul></li><li><span class="TLline"><a href="/medgen/167258" ref="tree=MeSH" title="MedGen record for Hypertensive renal disease">Hypertensive renal disease</a></span></li><li><span class="TLline"><a href="/medgen/884419" ref="tree=MeSH" title="MedGen record for Idiopathic Renal Papillary Necrosis">Idiopathic Renal Papillary Necrosis</a></span></li><li><span class="TLline"><a href="/medgen/11952" ref="tree=MeSH" title="MedGen record for Interstitial nephritis">Interstitial nephritis</a></span><ul><li><span class="TLline"><a href="/medgen/334716" ref="tree=MeSH" title="MedGen record for Acute tubulointerstitial nephritis">Acute tubulointerstitial nephritis</a></span></li><li><span class="TLline"><a href="/medgen/65957" ref="tree=MeSH" title="MedGen record for Chronic tubulointerstitial nephritis">Chronic tubulointerstitial nephritis</a></span></li></ul></li><li><span class="TLline"><a href="/medgen/473176" ref="tree=MeSH" title="MedGen record for Ischemic glomerulopathy">Ischemic glomerulopathy</a></span></li><li><span class="TLline"><a href="/medgen/853817" ref="tree=MeSH" title="MedGen record for Ischemic nephropathy">Ischemic nephropathy</a></span></li><li><span class="TLline"><a href="/medgen/7212" ref="tree=MeSH" title="MedGen record for Kidney papillary necrosis">Kidney papillary necrosis</a></span></li><li><span class="TLline"><a href="/medgen/536781" ref="tree=MeSH" title="MedGen record for Kidney Transplant Rejection">Kidney Transplant Rejection</a></span><ul><li><span class="TLline"><a href="/medgen/859709" ref="tree=MeSH" title="MedGen record for Acute Cellular Allograft Nephropathy">Acute Cellular Allograft Nephropathy</a></span></li><li><span class="TLline"><a href="/medgen/859708" ref="tree=MeSH" title="MedGen record for Acute Humoral Allograft Nephropathy">Acute Humoral Allograft Nephropathy</a></span></li></ul></li><li><span class="TLline"><a href="/medgen/881933" ref="tree=MeSH" title="MedGen record for Leptospirosis Nephropathy">Leptospirosis Nephropathy</a></span></li><li><span class="TLline"><a href="/medgen/887404" ref="tree=MeSH" title="MedGen record for Malignant Hypertensive Nephropathy">Malignant Hypertensive Nephropathy</a></span></li><li><span class="TLline"><a href="/medgen/541440" ref="tree=MeSH" title="MedGen record for Nephritic syndrome">Nephritic syndrome</a></span></li><li><span class="TLline"><a href="/medgen/14328" ref="tree=MeSH" title="MedGen record for Nephritis">Nephritis</a></span><ul><li><span class="TLline"><a href="/medgen/6616" ref="tree=MeSH" title="MedGen record for Glomerulonephritis">Glomerulonephritis</a></span></li><li><span class="TLline"><a href="/medgen/10305" ref="tree=MeSH" title="MedGen record for Hereditary nephritis">Hereditary nephritis</a></span></li><li><span class="TLline"><a href="/medgen/10656" ref="tree=MeSH" title="MedGen record for Perinephritis">Perinephritis</a></span></li><li><span class="TLline"><a href="/medgen/48268" ref="tree=MeSH" title="MedGen record for Pyelitis">Pyelitis</a></span></li><li><span class="TLline"><a href="/medgen/19590" ref="tree=MeSH" title="MedGen record for Pyelonephritis">Pyelonephritis</a></span></li></ul></li><li><span class="TLline"><a href="/medgen/10222" ref="tree=MeSH" title="MedGen record for Nephrocalcinosis">Nephrocalcinosis</a></span><ul><li><span class="TLline"><a href="/medgen/588417" ref="tree=MeSH" title="MedGen record for Cortical nephrocalcinosis">Cortical nephrocalcinosis</a></span></li><li><span class="TLline"><a href="/medgen/588418" ref="tree=MeSH" title="MedGen record for Medullary nephrocalcinosis">Medullary nephrocalcinosis</a></span></li><li><span class="TLline"><a href="/medgen/98014" ref="tree=MeSH" title="MedGen record for Microscopic nephrocalcinosis">Microscopic nephrocalcinosis</a></span></li></ul></li><li><span class="TLline"><a href="/medgen/98227" ref="tree=MeSH" title="MedGen record for Nephrolithiasis">Nephrolithiasis</a></span><ul><li><span class="TLline"><a href="/medgen/344578" ref="tree=MeSH" title="MedGen record for Calcium nephrolithiasis">Calcium nephrolithiasis</a></span></li><li><span class="TLline"><a href="/medgen/1054715" ref="tree=MeSH" title="MedGen record for Cystine nephrolithiasis">Cystine nephrolithiasis</a></span></li><li><span class="TLline"><a href="/medgen/568794" ref="tree=MeSH" title="MedGen record for Staghorn calculus">Staghorn calculus</a></span></li><li><span class="TLline"><a href="/medgen/866709" ref="tree=MeSH" title="MedGen record for Struvite nephrolithiasis">Struvite nephrolithiasis</a></span></li><li><span class="TLline"><a href="/medgen/140791" ref="tree=MeSH" title="MedGen record for Uric acid nephrolithiasis">Uric acid nephrolithiasis</a></span></li><li><span class="TLline"><a href="/medgen/376358" ref="tree=MeSH" title="MedGen record for Xanthine nephrolithiasis">Xanthine nephrolithiasis</a></span></li></ul></li><li><span class="TLline"><a href="/medgen/146912" ref="tree=MeSH" title="MedGen record for Nephronophthisis">Nephronophthisis</a></span><ul><li><span class="TLline"><a href="/medgen/355574" ref="tree=MeSH" title="MedGen record for Infantile nephronophthisis">Infantile nephronophthisis</a></span></li><li><span class="TLline"><a href="/medgen/1842314" ref="tree=MeSH" title="MedGen record for Late-onset nephronophthisis">Late-onset nephronophthisis</a></span></li><li><span class="TLline"><a href="/medgen/343406" ref="tree=MeSH" title="MedGen record for Nephronophthisis 1">Nephronophthisis 1</a></span></li><li><span class="TLline"><a href="/medgen/346809" ref="tree=MeSH" title="MedGen record for Nephronophthisis 3">Nephronophthisis 3</a></span></li><li><span class="TLline"><a href="/medgen/339667" ref="tree=MeSH" title="MedGen record for Nephronophthisis 4">Nephronophthisis 4</a></span></li><li><span class="TLline"><a href="/medgen/369409" ref="tree=MeSH" title="MedGen record for Nephronophthisis 7">Nephronophthisis 7</a></span></li><li><span class="TLline"><a href="/medgen/468521" ref="tree=MeSH" title="MedGen record for Nephronophthisis 8">Nephronophthisis 8</a></span></li><li><span class="TLline"><a href="/medgen/462538" ref="tree=MeSH" title="MedGen record for Nephronophthisis 9">Nephronophthisis 9</a></span></li><li><span class="TLline"><a href="/medgen/462146" ref="tree=MeSH" title="MedGen record for Nephronophthisis 11">Nephronophthisis 11</a></span></li></ul></li><li><span class="TLline"><a href="/medgen/881412" ref="tree=MeSH" title="MedGen record for Nephropathy Associated with Rhabdomyolysis">Nephropathy Associated with Rhabdomyolysis</a></span></li><li><span class="TLline"><a href="/medgen/625180" ref="tree=MeSH" title="MedGen record for Nephropathy caused by heavy metals">Nephropathy caused by heavy metals</a></span></li><li><span class="TLline"><a href="/medgen/14330" ref="tree=MeSH" title="MedGen record for Nephrosclerosis">Nephrosclerosis</a></span></li><li><span class="TLline"><a href="/medgen/10223" ref="tree=MeSH" title="MedGen record for Nephrosis">Nephrosis</a></span><ul><li><span class="TLline"><a href="/medgen/10307" ref="tree=MeSH" title="MedGen record for Lipoid nephrosis">Lipoid nephrosis</a></span></li><li><span class="TLline"><a href="/medgen/10308" ref="tree=MeSH" title="MedGen record for Nephrotic syndrome">Nephrotic syndrome</a></span></li></ul></li><li><span class="TLline"><a href="/medgen/235388" ref="tree=MeSH" title="MedGen record for Non-Neoplastic Kidney Disorder">Non-Neoplastic Kidney Disorder</a></span><ul><li><span class="TLline"><a href="/medgen/474887" ref="tree=MeSH" title="MedGen record for Arterionephrosclerosis">Arterionephrosclerosis</a></span></li><li><span class="TLline"><a href="/medgen/473458" ref="tree=MeSH" title="MedGen record for Chronic kidney disease">Chronic kidney disease</a></span></li><li><span class="TLline"><a href="/medgen/1384792" ref="tree=MeSH" title="MedGen record for Cystinosis">Cystinosis</a></span></li><li><span class="TLline"><a href="/medgen/888915" ref="tree=MeSH" title="MedGen record for Infundibular Stenosis">Infundibular Stenosis</a></span></li><li><span class="TLline"><a href="/medgen/11177" ref="tree=MeSH" title="MedGen record for Kidney failure">Kidney failure</a></span></li><li><span class="TLline"><a href="/medgen/510218" ref="tree=MeSH" title="MedGen record for Kidney hypertrophy">Kidney hypertrophy</a></span></li><li><span class="TLline"><a href="/medgen/508095" ref="tree=MeSH" title="MedGen record for Renal infarction">Renal infarction</a></span></li><li><span class="TLline"><a href="/medgen/233402" ref="tree=MeSH" title="MedGen record for Renal Pelvis Fibroepithelial Polyp">Renal Pelvis Fibroepithelial Polyp</a></span></li><li><span class="TLline"><a href="/medgen/78700" ref="tree=MeSH" title="MedGen record for Renal vascular disorder">Renal vascular disorder</a></span></li></ul></li><li><span class="TLline"><a href="/medgen/508456" ref="tree=MeSH" title="MedGen record for Obstructive nephropathy">Obstructive nephropathy</a></span></li><li><span class="TLline"><a href="/medgen/609100" ref="tree=MeSH" title="MedGen record for Oligomeganephronia">Oligomeganephronia</a></span></li><li><span class="TLline"><a href="/medgen/326534" ref="tree=MeSH" title="MedGen record for Proximal tubulopathy">Proximal tubulopathy</a></span><ul><li><span class="TLline"><a href="/medgen/868445" ref="tree=MeSH" title="MedGen record for Global proximal tubulopathy">Global proximal tubulopathy</a></span></li><li><span class="TLline"><a href="/medgen/1700527" ref="tree=MeSH" title="MedGen record for Light Chain Proximal Tubulopathy without Crystals">Light Chain Proximal Tubulopathy without Crystals</a></span></li><li><span class="TLline"><a href="/medgen/870722" ref="tree=MeSH" title="MedGen record for Non-acidotic proximal tubulopathy">Non-acidotic proximal tubulopathy</a></span></li></ul></li><li><span class="TLline"><a href="/medgen/890011" ref="tree=MeSH" title="MedGen record for Radiation Nephropathy">Radiation Nephropathy</a></span></li><li><span class="TLline"><a href="/medgen/886472" ref="tree=MeSH" title="MedGen record for Reflux Nephropathy">Reflux Nephropathy</a></span></li><li><span class="TLline"><a href="/medgen/48406" ref="tree=MeSH" title="MedGen record for Renal artery obstruction">Renal artery obstruction</a></span></li><li><span class="TLline"><a href="/medgen/9634" ref="tree=MeSH" title="MedGen record for Renal cortical necrosis">Renal cortical necrosis</a></span></li><li><span class="TLline"><a href="/medgen/5700" ref="tree=MeSH" title="MedGen record for Renal hypertension">Renal hypertension</a></span><ul><li><span class="TLline"><a href="/medgen/43786" ref="tree=MeSH" title="MedGen record for Renovascular hypertension">Renovascular hypertension</a></span></li></ul></li><li><span class="TLline"><a href="/medgen/332529" ref="tree=MeSH" title="MedGen record for Renal insufficiency">Renal insufficiency</a></span><ul><li><span class="TLline"><a href="/medgen/388570" ref="tree=MeSH" title="MedGen record for Acute kidney injury">Acute kidney injury</a></span></li><li><span class="TLline"><a href="/medgen/453248" ref="tree=MeSH" title="MedGen record for Cardio-renal syndrome">Cardio-renal syndrome</a></span></li><li><span class="TLline"><a href="/medgen/140787" ref="tree=MeSH" title="MedGen record for Chronic renal insufficiency">Chronic renal insufficiency</a></span></li><li><span class="TLline"><a href="/medgen/334717" ref="tree=MeSH" title="MedGen record for Reversible renal failure">Reversible renal failure</a></span></li></ul></li><li><span class="TLline"><a href="/medgen/5967" ref="tree=MeSH" title="MedGen record for Renal neoplasm">Renal neoplasm</a></span><ul><li><span class="TLline"><a href="/medgen/220422" ref="tree=MeSH" title="MedGen record for Benign cystic nephroma">Benign cystic nephroma</a></span></li><li><span class="TLline"><a href="/medgen/232356" ref="tree=MeSH" title="MedGen record for Childhood kidney neoplasm">Childhood kidney neoplasm</a></span></li><li><span class="TLline"><a href="/medgen/1388623" ref="tree=MeSH" title="MedGen record for Clear cell papillary renal cell carcinoma">Clear cell papillary renal cell carcinoma</a></span></li><li><span class="TLline"><a href="/medgen/868779" ref="tree=MeSH" title="MedGen record for Embryonal renal neoplasm">Embryonal renal neoplasm</a></span></li><li><span class="TLline"><a href="/medgen/69146" ref="tree=MeSH" title="MedGen record for Kidney angiomyolipoma">Kidney angiomyolipoma</a></span></li><li><span class="TLline"><a href="/medgen/96926" ref="tree=MeSH" title="MedGen record for Kidney benign neoplasm">Kidney benign neoplasm</a></span></li><li><span class="TLline"><a href="/medgen/1687868" ref="tree=MeSH" title="MedGen record for Kidney Germ Cell Tumor">Kidney Germ Cell Tumor</a></span></li><li><span class="TLline"><a href="/medgen/1684226" ref="tree=MeSH" title="MedGen record for Kidney Mixed Epithelial and Stromal Tumor Family">Kidney Mixed Epithelial and Stromal Tumor Family</a></span></li><li><span class="TLline"><a href="/medgen/1672808" ref="tree=MeSH" title="MedGen record for Kidney Neuroendocrine Neoplasm">Kidney Neuroendocrine Neoplasm</a></span></li><li><span class="TLline"><a href="/medgen/149263" ref="tree=MeSH" title="MedGen record for Malignant tumor of kidney">Malignant tumor of kidney</a></span></li><li><span class="TLline"><a href="/medgen/64620" ref="tree=MeSH" title="MedGen record for Mesoblastic nephroma">Mesoblastic nephroma</a></span></li><li><span class="TLline"><a href="/medgen/87547" ref="tree=MeSH" title="MedGen record for Multilocular clear cell renal cell carcinoma">Multilocular clear cell renal cell carcinoma</a></span></li><li><span class="TLline"><a href="/medgen/10221" ref="tree=MeSH" title="MedGen record for Nephroblastoma">Nephroblastoma</a></span></li><li><span class="TLline"><a href="/medgen/91094" ref="tree=MeSH" title="MedGen record for Oncocytoma of kidney">Oncocytoma of kidney</a></span></li><li><span class="TLline"><a href="/medgen/766" ref="tree=MeSH" title="MedGen record for Renal cell carcinoma">Renal cell carcinoma</a></span></li><li><span class="TLline"><a href="/medgen/577332" ref="tree=MeSH" title="MedGen record for Renal cortical adenoma">Renal cortical adenoma</a></span></li><li><span class="TLline"><a href="/medgen/870535" ref="tree=MeSH" title="MedGen record for Renal pelvic carcinoma">Renal pelvic carcinoma</a></span></li><li><span class="TLline"><a href="/medgen/138049" ref="tree=MeSH" title="MedGen record for Renal pelvis neoplasm">Renal pelvis neoplasm</a></span></li><li><span class="TLline"><a href="/medgen/728084" ref="tree=MeSH" title="MedGen record for Renal transitional cell carcinoma">Renal transitional cell carcinoma</a></span></li></ul></li><li><span class="TLline"><a href="/medgen/465238" ref="tree=MeSH" title="MedGen record for Renal nutcracker syndrome">Renal nutcracker syndrome</a></span></li><li><span class="TLline"><a href="/medgen/21728" ref="tree=MeSH" title="MedGen record for Renal tuberculosis">Renal tuberculosis</a></span></li><li><span class="TLline"><a href="/medgen/19728" ref="tree=MeSH" title="MedGen record for Renal tubular transport disease">Renal tubular transport disease</a></span><ul><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/168056" ref="tree=MeSH" title="MedGen record for Dent disease">Dent disease</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/5713" ref="tree=MeSH" title="MedGen record for Familial Hypophosphatemias">Familial Hypophosphatemias</a></span></li><li><span class="TLline"><a href="/medgen/757652" ref="tree=MeSH" title="MedGen record for Familial renal glucosuria">Familial renal glucosuria</a></span></li><li><span class="TLline"><a href="/medgen/4653" ref="tree=MeSH" title="MedGen record for Fanconi syndrome">Fanconi syndrome</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/18145" ref="tree=MeSH" title="MedGen record for Lowe syndrome">Lowe syndrome</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/254" ref="tree=MeSH" title="MedGen record for Renal aminoaciduria">Renal aminoaciduria</a></span></li><li><span class="TLline"><a href="/medgen/90" ref="tree=MeSH" title="MedGen record for Renal tubular acidosis">Renal tubular acidosis</a></span></li></ul></li><li><span class="TLline"><a href="/medgen/883858" ref="tree=MeSH" title="MedGen record for Schistosomiasis Nephropathy">Schistosomiasis Nephropathy</a></span></li><li><span class="TLline"><a href="/medgen/536792" ref="tree=MeSH" title="MedGen record for Sickle cell nephropathy">Sickle cell nephropathy</a></span></li><li><span class="TLline"><a href="/medgen/12008" ref="tree=MeSH" title="MedGen record for Uremia">Uremia</a></span><ul><li><span class="TLline"><a href="/medgen/116608" ref="tree=MeSH" title="MedGen record for Azotemia">Azotemia</a></span></li></ul></li><li><span class="TLline"><a href="/medgen/21958" ref="tree=MeSH" title="MedGen record for Zellweger spectrum disorders">Zellweger spectrum disorders</a></span></li></ul></li><li><span class="TLline"><a href="/medgen/869314" ref="tree=MeSH" title="MedGen record for Low alkaline phosphatase of renal origin">Low alkaline phosphatase of renal origin</a></span></li><li><span class="TLline"><a href="/medgen/57484" ref="tree=MeSH" title="MedGen record for Renal tubular dysfunction">Renal tubular dysfunction</a></span><ul><li><span class="TLline"><a href="/medgen/869158" ref="tree=MeSH" title="MedGen record for Abnormal renal tubular resorption">Abnormal renal tubular resorption</a></span><ul><li><span class="TLline"><a href="/medgen/870207" ref="tree=MeSH" title="MedGen record for Impaired histidine renal tubular absorption">Impaired histidine renal tubular absorption</a></span></li><li><span class="TLline"><a href="/medgen/395351" ref="tree=MeSH" title="MedGen record for Impaired renal concentrating ability">Impaired renal concentrating ability</a></span></li><li><span class="TLline"><a href="/medgen/1783147" ref="tree=MeSH" title="MedGen record for Impaired renal tubular reabsorption of bicarbonate">Impaired renal tubular reabsorption of bicarbonate</a></span></li><li><span class="TLline"><a href="/medgen/375869" ref="tree=MeSH" title="MedGen record for Impaired renal tubular reabsorption of chloride">Impaired renal tubular reabsorption of chloride</a></span></li><li><span class="TLline"><a href="/medgen/1815094" ref="tree=MeSH" title="MedGen record for Impaired renal tubular reabsorption of glucose">Impaired renal tubular reabsorption of glucose</a></span></li><li><span class="TLline"><a href="/medgen/1815093" ref="tree=MeSH" title="MedGen record for Impaired renal tubular reabsorption of low molecular weight protein">Impaired renal tubular reabsorption of low molecular weight protein</a></span></li><li><span class="TLline"><a href="/medgen/1778245" ref="tree=MeSH" title="MedGen record for Impaired renal tubular reabsorption of magnesium">Impaired renal tubular reabsorption of magnesium</a></span></li><li><span class="TLline"><a href="/medgen/1815096" ref="tree=MeSH" title="MedGen record for Impaired renal tubular reabsorption of phosphate">Impaired renal tubular reabsorption of phosphate</a></span></li><li><span class="TLline"><a href="/medgen/1815095" ref="tree=MeSH" title="MedGen record for Impaired renal tubular reabsorption of sodium">Impaired renal tubular reabsorption of sodium</a></span></li><li><span class="TLline"><a href="/medgen/1781031" ref="tree=MeSH" title="MedGen record for Impaired renal tubular reabsorption of uric acid">Impaired renal tubular reabsorption of uric acid</a></span></li><li><span class="TLline"><a href="/medgen/368914" ref="tree=MeSH" title="MedGen record for Increased renal tubular phosphate reabsorption">Increased renal tubular phosphate reabsorption</a></span></li><li><span class="TLline"><a href="/medgen/341765" ref="tree=MeSH" title="MedGen record for Primary Fanconi syndrome">Primary Fanconi syndrome</a></span></li></ul></li><li><span class="TLline"><a href="/medgen/1375627" ref="tree=MeSH" title="MedGen record for Acquired monoclonal Ig light chain-associated Fanconi syndrome">Acquired monoclonal Ig light chain-associated Fanconi syndrome</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/1830116" ref="tree=MeSH" title="MedGen record for Atypical Fanconi syndrome-neonatal hyperinsulinism syndrome">Atypical Fanconi syndrome-neonatal hyperinsulinism syndrome</a></span></li><li><span class="TLline"><a href="/medgen/167082" ref="tree=MeSH" title="MedGen record for Cataract-nephropathy-encephalopathy syndrome">Cataract-nephropathy-encephalopathy syndrome</a></span></li><li><span class="TLline"><a href="/medgen/8226" ref="tree=MeSH" title="MedGen record for Cystinuria">Cystinuria</a></span><ul><li><span class="TLline"><a href="/medgen/347441" ref="tree=MeSH" title="MedGen record for Cystinuria type A">Cystinuria type A</a></span></li><li><span class="TLline"><a href="/medgen/347442" ref="tree=MeSH" title="MedGen record for Cystinuria type B">Cystinuria type B</a></span></li></ul></li><li><span class="TLline"><a href="/medgen/1680754" ref="tree=MeSH" title="MedGen record for Dominant hypophosphatemia with nephrolithiasis or osteoporosis">Dominant hypophosphatemia with nephrolithiasis or osteoporosis</a></span></li><li><span class="TLline"><a href="/medgen/411243" ref="tree=MeSH" title="MedGen record for EAST syndrome">EAST syndrome</a></span></li><li><span class="TLline"><a href="/medgen/1843381" ref="tree=MeSH" title="MedGen record for EGF-related primary hypomagnesemia with intellectual disability">EGF-related primary hypomagnesemia with intellectual disability</a></span></li><li><span class="TLline"><a href="/medgen/1843047" ref="tree=MeSH" title="MedGen record for Familial primary hypomagnesemia with hypercalciuria and nephrocalcinosis">Familial primary hypomagnesemia with hypercalciuria and nephrocalcinosis</a></span><ul><li><span class="TLline"><a href="/medgen/120640" ref="tree=MeSH" title="MedGen record for Primary hypomagnesemia">Primary hypomagnesemia</a></span></li><li><span class="TLline"><a href="/medgen/1648449" ref="tree=MeSH" title="MedGen record for Renal hypomagnesemia 5 with ocular involvement">Renal hypomagnesemia 5 with ocular involvement</a></span></li></ul></li><li><span class="TLline"><a href="/medgen/1643078" ref="tree=MeSH" title="MedGen record for Familial renal hypouricemia">Familial renal hypouricemia</a></span><ul><li><span class="TLline"><a href="/medgen/141632" ref="tree=MeSH" title="MedGen record for Dalmatian hypouricemia">Dalmatian hypouricemia</a></span></li><li><span class="TLline"><a href="/medgen/436974" ref="tree=MeSH" title="MedGen record for Hypouricemia, renal, 2">Hypouricemia, renal, 2</a></span></li></ul></li><li><span class="TLline"><a href="/medgen/1843117" ref="tree=MeSH" title="MedGen record for Gitelman-like kidney tubulopathy due to mitochondrial DNA mutation">Gitelman-like kidney tubulopathy due to mitochondrial DNA mutation</a></span></li><li><span class="TLline"><a href="/medgen/1621482" ref="tree=MeSH" title="MedGen record for HELIX syndrome">HELIX syndrome</a></span></li><li><span class="TLline"><a href="/medgen/1650300" ref="tree=MeSH" title="MedGen record for Hypertrophic cardiomyopathy and renal tubular disease due to mitochondrial DNA mutation">Hypertrophic cardiomyopathy and renal tubular disease due to mitochondrial DNA mutation</a></span></li><li><span class="TLline"><a href="/medgen/462559" ref="tree=MeSH" title="MedGen record for Hyperuricemia, pulmonary hypertension, renal failure, alkalosis syndrome">Hyperuricemia, pulmonary hypertension, renal failure, alkalosis syndrome</a></span></li><li><span class="TLline"><a href="/medgen/1433919" ref="tree=MeSH" title="MedGen record for Idiopathic inherited hypercalciuria">Idiopathic inherited hypercalciuria</a></span></li><li><span class="TLline"><a href="/medgen/355596" ref="tree=MeSH" title="MedGen record for Intestinal hypomagnesemia 1">Intestinal hypomagnesemia 1</a></span></li><li><span class="TLline"><a href="/medgen/930824" ref="tree=MeSH" title="MedGen record for Isolated autosomal dominant hypomagnesemia, Glaudemans type">Isolated autosomal dominant hypomagnesemia, Glaudemans type</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><ul><li><span class="TLline"><a href="/medgen/1648057" ref="tree=MeSH" title="MedGen record for Asphyxiating thoracic dystrophy 1">Asphyxiating thoracic dystrophy 1</a></span></li><li><span class="TLline"><a href="/medgen/370804" ref="tree=MeSH" title="MedGen record for Asphyxiating thoracic dystrophy 2">Asphyxiating thoracic dystrophy 2</a></span></li><li><span class="TLline"><a href="/medgen/19860" ref="tree=MeSH" title="MedGen record for Asphyxiating thoracic dystrophy 3">Asphyxiating thoracic dystrophy 3</a></span></li><li><span class="TLline"><a href="/medgen/462535" ref="tree=MeSH" title="MedGen record for Asphyxiating thoracic dystrophy 4">Asphyxiating thoracic dystrophy 4</a></span></li><li><span class="TLline"><a href="/medgen/482228" ref="tree=MeSH" title="MedGen record for Asphyxiating thoracic dystrophy 5">Asphyxiating thoracic dystrophy 5</a></span></li></ul></li><li><span class="TLline"><a href="/medgen/1674910" ref="tree=MeSH" title="MedGen record for Mitochondrial DNA depletion syndrome, hepatocerebrorenal form">Mitochondrial DNA depletion syndrome, hepatocerebrorenal form</a></span></li><li><span class="TLline"><a href="/medgen/387791" ref="tree=MeSH" title="MedGen record for Nephrogenic diabetes insipidus-intracranial calcification syndrome">Nephrogenic diabetes insipidus-intracranial calcification syndrome</a></span></li><li><span class="TLline"><a href="/medgen/336877" ref="tree=MeSH" title="MedGen record for Nephrogenic syndrome of inappropriate antidiuresis">Nephrogenic syndrome of inappropriate antidiuresis</a></span></li><li><span class="TLline"><a href="/medgen/1842330" ref="tree=MeSH" title="MedGen record for Primary hypomagnesemia-generalized seizures-intellectual disability-obesity syndrome">Primary hypomagnesemia-generalized seizures-intellectual disability-obesity syndrome</a></span></li><li><span class="TLline"><a href="/medgen/1621949" ref="tree=MeSH" title="MedGen record for Psychomotor regression-oculomotor apraxia-movement disorder-nephropathy syndrome">Psychomotor regression-oculomotor apraxia-movement disorder-nephropathy syndrome</a></span></li><li><span class="TLline"><a href="/medgen/320542" ref="tree=MeSH" title="MedGen record for Renal hypomagnesemia 2">Renal hypomagnesemia 2</a></span></li><li><span class="TLline"><a href="/medgen/870273" ref="tree=MeSH" title="MedGen record for Renal tubular lysine transport defect">Renal tubular lysine transport defect</a></span></li><li><span class="TLline"><a href="/medgen/930068" ref="tree=MeSH" title="MedGen record for Tubular renal disease-cardiomyopathy syndrome">Tubular renal disease-cardiomyopathy syndrome</a></span></li><li><span class="TLline"><a href="/medgen/334715" ref="tree=MeSH" title="MedGen record for Tubulointerstitial nephritis and uveitis syndrome">Tubulointerstitial nephritis and uveitis syndrome</a></span></li><li><span class="TLline"><a href="/medgen/226893" ref="tree=MeSH" title="MedGen record for Tumor-induced osteomalacia">Tumor-induced osteomalacia</a></span></li></ul></li></ul></li></ul></li></ul></li></ul></li></ul></li></ul></li></ul></li></ul></div></div></div></div>
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<div class="portlet_head mgSectionHead ui-widget-header"><h1 class="nl" id="Conditions_with_this_feature">Conditions with this feature</h1><a sid="112" href="#" class="portlet_shutter" title="Show/hide content"></a></div>
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<div class="divPopper rprt" id="rdis_41678"><div><strong>Familial dysautonomia</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>41678</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.">C0013364</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
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<div class="spaceAbove">Familial dysautonomia, which affects the development and survival of sensory, sympathetic, and parasympathetic neurons, is a debilitating disorder present from birth. Neuronal degeneration progresses throughout life. Affected individuals have gastrointestinal dysfunction, autonomic crises (i.e., hypertensive vomiting attacks), recurrent pneumonia, altered pain sensitivity, altered temperature perception, and blood pressure instability. Hypotonia contributes to delay in acquisition of motor milestones. Optic neuropathy results in progressive vision loss. Older individuals often have a broad-based and ataxic gait that deteriorates over time. Developmental delay / intellectual disability occur in about 21% of individuals. Life expectancy is decreased.</div>
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<div class="spaceAbove nowrap">See: <a href="/medgen/41678">Condition Record</a></div></div>
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<div class="divPopper rprt" id="rdis_11161"><div><strong>Phytanic acid storage disease</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>11161</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.">C0034960</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
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<div class="spaceAbove">Adult Refsum disease (ARD is associated with elevated plasma phytanic acid levels, late childhood-onset (or later) retinitis pigmentosa, and variable combinations of anosmia, polyneuropathy, deafness, ataxia, and ichthyosis. Onset of symptoms ranges from age seven months to older than age 50 years. Cardiac arrhythmia and heart failure caused by cardiomyopathy are potentially severe health problems that develop later in life.</div>
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<div class="spaceAbove nowrap">See: <a href="/medgen/11161">Condition Record</a></div></div>
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<div class="divPopper rprt" id="rdis_224783"><div><strong>Upshaw-Schulman syndrome</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>224783</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.">C1268935</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
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<div class="spaceAbove">Hereditary thrombotic thrombocytopenic purpura (TTP), also known as Upshaw-Schulman syndrome (USS), is a rare autosomal recessive thrombotic microangiopathy (TMA). Clinically, acute phases of TTP are defined by microangiopathic mechanical hemolytic anemia, severe thrombocytopenia, and visceral ischemia. Hereditary TTP makes up 5% of TTP cases and is caused mostly by biallelic mutation in the ADAMTS13 gene, or in very rare cases, by monoallelic ADAMTS13 mutation associated with a cluster of single-nucleotide polymorphisms (SNPs); most cases of all TTP (95%) are acquired via an autoimmune mechanism (see 188030). Hereditary TTP is more frequent among child-onset TTP compared with adult-onset TTP, and its clinical presentation is significantly different as a function of its age of onset. Child-onset TTP usually starts in the neonatal period with hematological features and severe jaundice. In contrast, almost all cases of adult-onset hereditary TTP are unmasked during the first pregnancy of a woman whose disease was silent during childhood (summary by Joly et al., 2018).</div>
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<div class="spaceAbove nowrap">See: <a href="/medgen/224783">Condition Record</a></div></div>
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<div class="divPopper rprt" id="rdis_332086"><div><strong>Systemic lupus erythematosus, susceptibility to, 6</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>332086</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.">C1835919</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Finding</dd></dl></div></div></div>
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<div class="spaceAbove">SLE may first appear as extreme tiredness (fatigue), a vague feeling of discomfort or illness (malaise), fever, loss of appetite, and weight loss. Most affected individuals also have joint pain, typically affecting the same joints on both sides of the body, and muscle pain and weakness. Skin problems are common in SLE. A characteristic feature is a flat red rash across the cheeks and bridge of the nose, called a "butterfly rash" because of its shape. The rash, which generally does not hurt or itch, often appears or becomes more pronounced when exposed to sunlight. Other skin problems that may occur in SLE include calcium deposits under the skin (calcinosis), damaged blood vessels (vasculitis) in the skin, and tiny red spots called petechiae. Petechiae are caused by a shortage of cells involved in clotting (platelets), which leads to bleeding under the skin. Affected individuals may also have hair loss (alopecia) and open sores (ulcerations) in the moist lining (mucosae) of the mouth, nose, or, less commonly, the genitals.\n\nSystemic lupus erythematosus (SLE) is a chronic disease that causes inflammation in connective tissues, such as cartilage and the lining of blood vessels, which provide strength and flexibility to structures throughout the body. The signs and symptoms of SLE vary among affected individuals, and can involve many organs and systems, including the skin, joints, kidneys, lungs, central nervous system, and blood-forming (hematopoietic) system. SLE is one of a large group of conditions called autoimmune disorders that occur when the immune system attacks the body's own tissues and organs.\n\nAbout a third of people with SLE develop kidney disease (nephritis). Heart problems may also occur in SLE, including inflammation of the sac-like membrane around the heart (pericarditis) and abnormalities of the heart valves, which control blood flow in the heart. Heart disease caused by fatty buildup in the blood vessels (atherosclerosis), which is very common in the general population, is even more common in people with SLE. The inflammation characteristic of SLE can also damage the nervous system, and may result in abnormal sensation and weakness in the limbs (peripheral neuropathy); seizures; stroke; and difficulty processing, learning, and remembering information (cognitive impairment). Anxiety and depression are also common in SLE.\n\nPeople with SLE have episodes in which the condition gets worse (exacerbations) and other times when it gets better (remissions). Overall, SLE gradually gets worse over time, and damage to the major organs of the body can be life-threatening.</div>
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<div class="spaceAbove nowrap">See: <a href="/medgen/332086">Condition Record</a></div></div>
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<div class="divPopper rprt" id="rdis_333429"><div><strong>X-linked diffuse leiomyomatosis-Alport syndrome</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>333429</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.">C1839884</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">A rare renal disease characterized by the association of X-linked Alport syndrome (glomerular nephropathy, sensorineural deafness and ocular anomalies) and benign proliferation of visceral smooth muscle cells along the gastrointestinal, respiratory, and female genital tracts and clinically manifests with dysphagia, dyspnea, cough, stridor, postprandial vomiting, retrosternal or epigastric pain, recurrent pneumonia, and clitoral hypertrophy in females.</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/333429">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_343814"><div><strong>Cryoglobulinemic vasculitis</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>343814</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.">C1852456</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">A rare immune complex-mediated vasculitis characterized by the presence of circulating cryoprecipitable immune complexes in the serum, manifesting clinically with the classical triad of purpura, weakness and arthralgia.</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/343814">Condition Record</a></div></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_343814" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Cryoglobulinemic vasculitis</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_41678" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Familial dysautonomia</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_11161" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Phytanic acid storage disease</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_332086" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Systemic lupus erythematosus, susceptibility to, 6</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_224783" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Upshaw-Schulman syndrome</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_333429" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">X-linked diffuse leiomyomatosis-Alport syndrome</a></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/31706619">Potassium homeostasis and management of dyskalemia in kidney diseases: conclusions from a Kidney Disease: Improving Global Outcomes (KDIGO) Controversies Conference.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Clase CM,
|
||
Carrero JJ,
|
||
Ellison DH,
|
||
Grams ME,
|
||
Hemmelgarn BR,
|
||
Jardine MJ,
|
||
Kovesdy CP,
|
||
Kline GA,
|
||
Lindner G,
|
||
Obrador GT,
|
||
Palmer BF,
|
||
Cheung M,
|
||
Wheeler DC,
|
||
Winkelmayer WC,
|
||
Pecoits-Filho R;
|
||
Conference Participants</span><br />
|
||
<span class="medgenPMjournal">Kidney Int</span>
|
||
2020 Jan;97(1):42-61.
|
||
Epub 2019 Oct 10
|
||
doi: 10.1016/j.kint.2019.09.018.
|
||
<span class="bold">PMID: </span><a href="/pubmed/31706619" target="_blank">31706619</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/29108899">Kallmann syndrome: phenotype and genotype of hypogonadotropic hypogonadism.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Stamou MI,
|
||
Georgopoulos NA</span><br />
|
||
<span class="medgenPMjournal">Metabolism</span>
|
||
2018 Sep;86:124-134.
|
||
Epub 2017 Nov 3
|
||
doi: 10.1016/j.metabol.2017.10.012.
|
||
<span class="bold">PMID: </span><a href="/pubmed/29108899" target="_blank">29108899</a><a href="/pmc/articles/PMC5934335" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/24685669">2014 AHA/ACC/HRS guideline for the management of patients with atrial fibrillation: a report of the American College of Cardiology/American Heart Association Task Force on Practice Guidelines and the Heart Rhythm Society.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">January CT,
|
||
Wann LS,
|
||
Alpert JS,
|
||
Calkins H,
|
||
Cigarroa JE,
|
||
Cleveland JC Jr,
|
||
Conti JB,
|
||
Ellinor PT,
|
||
Ezekowitz MD,
|
||
Field ME,
|
||
Murray KT,
|
||
Sacco RL,
|
||
Stevenson WG,
|
||
Tchou PJ,
|
||
Tracy CM,
|
||
Yancy CW;
|
||
American College of Cardiology/American Heart Association Task Force on Practice Guidelines</span><br />
|
||
<span class="medgenPMjournal">J Am Coll Cardiol</span>
|
||
2014 Dec 2;64(21):e1-76.
|
||
Epub 2014 Mar 28
|
||
doi: 10.1016/j.jacc.2014.03.022.
|
||
<span class="bold">PMID: </span><a href="/pubmed/24685669" target="_blank">24685669</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=(abnormal%20renal%20physiology)%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 (164)</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/1442756">The kidney in hypertensive pregnancies--victim and villain.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Brown MA,
|
||
Whitworth JA</span><br />
|
||
<span class="medgenPMjournal">Am J Kidney Dis</span>
|
||
1992 Nov;20(5):427-42.
|
||
doi: 10.1016/s0272-6386(12)70255-x.
|
||
<span class="bold">PMID: </span><a href="/pubmed/1442756" target="_blank">1442756</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Abnormal%20renal%20physiology%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 (1)</a></div><h3 class="subhead">Diagnosis</h3>
|
||
<div class="nl"><a target="_blank" href="/pubmed/32843431">Clinical utility of ultra-rapid whole-genome sequencing in an infant with atypical presentation of WT1-associated nephrotic syndrome type 4.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Sanford E,
|
||
Wong T,
|
||
Ellsworth KA,
|
||
Ingulli E,
|
||
Kingsmore SF</span><br />
|
||
<span class="medgenPMjournal">Cold Spring Harb Mol Case Stud</span>
|
||
2020 Aug;6(4)
|
||
Epub 2020 Aug 25
|
||
doi: 10.1101/mcs.a005470.
|
||
<span class="bold">PMID: </span><a href="/pubmed/32843431" target="_blank">32843431</a><a href="/pmc/articles/PMC7476414" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Abnormal%20renal%20physiology%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 (1)</a></div></div>
|
||
</div>
|
||
</div></div></div></div></div></div></div>
|
||
<div id="messagearea_bottom">
|
||
|
||
</div>
|
||
<div class=" bottom">
|
||
|
||
</div>
|
||
|
||
</div>
|
||
</div>
|
||
<div class="supplemental col three_col last">
|
||
<h2 class="offscreen_noflow">Supplemental Content</h2>
|
||
|
||
<div>
|
||
|
||
<!-- MedGen supplemental column starts here -->
|
||
<div class="rightCol mgCol">
|
||
<div class="portlet mgSection" id="ID_113">
|
||
<div class="portlet_head mgSectionHead ui-widget-header"><h1 class="nl" id="Table_of_contents">Table of contents</h1><a sid="113" href="#" class="portlet_shutter" title="Show/hide content"></a></div>
|
||
<div class="portlet_content ln"><ul id="my-toc"></ul></div>
|
||
</div>
|
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|
||
<div class="portlet mgSection" id="ID_106">
|
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<div class="portlet_head mgSectionHead ui-widget-header"><h1 class="nl" id="Genetic_Testing_Registry">Genetic Testing Registry</h1><a sid="106" href="#" class="portlet_shutter" title="Show/hide content"></a></div>
|
||
<div class="portlet_content ln"><ul><li><a href="/gtr/tests?term=C0151746%5bDISCUI%5d&filter=method%3A2%5F8" target="_blank">Deletion/duplication analysis (1)</a></li>
|
||
<li><a href="/gtr/tests?term=C0151746%5bDISCUI%5d&filter=method%3A2%5F7" target="_blank">Sequence analysis of the entire coding region (1)</a></li>
|
||
<li class="portletSeeAll portletSeeAllPad"><total><a href="/gtr/tests?term=C0151746%5bDISCUI%5d" target="_blank">See all (1)</a></total></li>
|
||
</ul></div>
|
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</div>
|
||
|
||
<div class="portlet mgSection" id="ID_119">
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<div class="portlet_head mgSectionHead ui-widget-header"><h1 class="nl" id="Clinical_resources">Clinical resources</h1><a sid="119" href="#" class="portlet_shutter" title="Show/hide content"></a></div>
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<div class="portlet_content ln"><ul><li><a href="https://clinicaltrials.gov/search?cond=Abnormal%20renal%20physiology" target="_blank">ClinicalTrials.gov</a></li></ul></div>
|
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</div>
|
||
|
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<div class="portlet mgSection" id="ID_121">
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<div class="portlet_head mgSectionHead ui-widget-header"><h1 class="nl" id="Practice_guidelines">Practice guidelines</h1><a sid="121" href="#" class="portlet_shutter" title="Show/hide content"></a></div>
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||
<div class="portlet_content ln"><ul class="a_poppers"><li><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=(abnormal%20renal%20physiology)%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">PubMed</a><div class="help-popup">See practice and clinical guidelines in PubMed. The search results may include broader topics and may not capture all published guidelines. See the <a href="/medgen/docs/faq/" title="Frequently asked questions" target="_blank">FAQ</a> for details.</div></li><li><a target="_blank" href="/books/?term=((%22clinical%20guidelines%22%5BResource%20Type%5D)%20OR%20%22practice%20guideline%22%5BPublication%20Type%5D)%20AND%20(%22Abnormal%20renal%20physiology%22)">Bookshelf</a><div class="help-popup">See practice and clinical guidelines in NCBI Bookshelf. The search results may include broader topics and may not capture all published guidelines. See the <a href="/medgen/docs/faq/" title="Frequently asked questions" target="_blank">FAQ</a> for details.</div></li></ul></div>
|
||
</div>
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|
||
<div class="portlet mgSection" id="ID_116">
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<div class="portlet_head mgSectionHead ui-widget-header"><h1 class="nl" id="Consumer_resources">Consumer resources</h1><a sid="116" href="#" class="portlet_shutter" title="Show/hide content"></a></div>
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<div class="portlet_content ln"><ul><li><a href="https://vsearch.nlm.nih.gov/vivisimo/cgi-bin/query-meta?v:project=medlineplus&query=Abnormal%20renal%20physiology" target="_blank">MedlinePlus</a></li></ul></div>
|
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</div>
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<div class="portlet brieflink">
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<div class="portlet_head">
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<div class="portlet_title">
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<h3>Reviews</h3>
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<p><a href="https://www.nlm.nih.gov/web_policies.html" class="text-white">Web Policies</a><br />
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<p><a class="supportLink text-white" href="https://support.nlm.nih.gov/">Help</a><br />
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