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<span>Genetic Conditions: T</span>
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<h1>Genetic Conditions: T</h1>
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<p>Explore the signs and symptoms, genetic cause, and inheritance pattern of various health conditions.</p>
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<span class='blue-label'>Other genetic conditions A-Z</span>
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<ul class="alpha-links">
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<li><a href="https://medlineplus.gov/genetics/condition-0/" data-alpha="0-9">0-9</a></li>
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<li><a href="https://medlineplus.gov/genetics/condition/" data-alpha="A">A</a></li>
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<li><a href="https://medlineplus.gov/genetics/condition-b/" data-alpha="B">B</a></li>
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<li><a href="https://medlineplus.gov/genetics/condition-c/" data-alpha="C">C</a></li>
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<li><a href="https://medlineplus.gov/genetics/condition-d/" data-alpha="D">D</a></li>
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<li><a href="https://medlineplus.gov/genetics/condition-e/" data-alpha="E">E</a></li>
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<li><a href="https://medlineplus.gov/genetics/condition-f/" data-alpha="F">F</a></li>
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<li><a href="https://medlineplus.gov/genetics/condition-g/" data-alpha="G">G</a></li>
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<li><a href="https://medlineplus.gov/genetics/condition-h/" data-alpha="H">H</a></li>
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<li><a href="https://medlineplus.gov/genetics/condition-i/" data-alpha="I">I</a></li>
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<li><a href="https://medlineplus.gov/genetics/condition-j/" data-alpha="J">J</a></li>
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<li><a href="https://medlineplus.gov/genetics/condition-k/" data-alpha="K">K</a></li>
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<li><a href="https://medlineplus.gov/genetics/condition-l/" data-alpha="L">L</a></li>
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<li><a href="https://medlineplus.gov/genetics/condition-m/" data-alpha="M">M</a></li>
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<li><a href="https://medlineplus.gov/genetics/condition-n/" data-alpha="N">N</a></li>
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<li><a href="https://medlineplus.gov/genetics/condition-o/" data-alpha="O">O</a></li>
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<li><a href="https://medlineplus.gov/genetics/condition-p/" data-alpha="P">P</a></li>
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<li><a href="https://medlineplus.gov/genetics/condition-q/" data-alpha="Q">Q</a></li>
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<li><a href="https://medlineplus.gov/genetics/condition-r/" data-alpha="R">R</a></li>
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<li><a href="https://medlineplus.gov/genetics/condition-s/" data-alpha="S">S</a></li>
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<li><span class="active">T</span></li>
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<li><a href="https://medlineplus.gov/genetics/condition-u/" data-alpha="U">U</a></li>
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<li><a href="https://medlineplus.gov/genetics/condition-v/" data-alpha="V">V</a></li>
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||
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<li><a href="https://medlineplus.gov/genetics/condition-w/" data-alpha="W">W</a></li>
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<li><a href="https://medlineplus.gov/genetics/condition-x/" data-alpha="X">X</a></li>
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|
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<li><a href="https://medlineplus.gov/genetics/condition-y/" data-alpha="Y">Y</a></li>
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<li><a href="https://medlineplus.gov/genetics/condition-z/" data-alpha="Z">Z</a></li>
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</section>
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<section>
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|
||
<ul class="withident breaklist">
|
||
|
||
<li>T cell-negative, B cell-positive, NK cell-negative SCID, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/jak3-deficient-severe-combined-immunodeficiency/">JAK3-deficient severe combined immunodeficiency</a></li>
|
||
|
||
|
||
<li>T-B+ severe combined immunodeficiency due to JAK3 deficiency, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/jak3-deficient-severe-combined-immunodeficiency/">JAK3-deficient severe combined immunodeficiency</a></li>
|
||
|
||
|
||
<li><a href="https://medlineplus.gov/genetics/condition/t-cell-immunodeficiency-congenital-alopecia-and-nail-dystrophy/">T-cell immunodeficiency, congenital alopecia, and nail dystrophy</a></li>
|
||
|
||
<li>T1D, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/type-1-diabetes/">Type 1 diabetes</a></li>
|
||
|
||
|
||
<li>T2 deficiency, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/beta-ketothiolase-deficiency/">Beta-ketothiolase deficiency</a></li>
|
||
|
||
|
||
<li>T2D, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/type-2-diabetes/">Type 2 diabetes</a></li>
|
||
|
||
|
||
<li>TAA, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/familial-thoracic-aortic-aneurysm-and-dissection/">Familial thoracic aortic aneurysm and dissection</a></li>
|
||
|
||
|
||
<li>TAAD, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/familial-thoracic-aortic-aneurysm-and-dissection/">Familial thoracic aortic aneurysm and dissection</a></li>
|
||
|
||
|
||
<li>TACH, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/pol-iii-related-leukodystrophy/">Pol III-related leukodystrophy</a></li>
|
||
|
||
|
||
<li>TAM, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/tubular-aggregate-myopathy/">Tubular aggregate myopathy</a></li>
|
||
|
||
|
||
<li><a href="https://medlineplus.gov/genetics/condition/tangier-disease/">Tangier disease</a></li>
|
||
|
||
<li>Tangier disease neuropathy, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/tangier-disease/">Tangier disease</a></li>
|
||
|
||
|
||
<li>Tangier hereditary neuropathy, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/tangier-disease/">Tangier disease</a></li>
|
||
|
||
|
||
<li>Tapetoretinal degeneration, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/cone-rod-dystrophy/">Cone-rod dystrophy</a></li>
|
||
|
||
|
||
<li>Tapetoretinal degeneration, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/retinitis-pigmentosa/">Retinitis pigmentosa</a></li>
|
||
|
||
|
||
<li>TAR syndrome, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/thrombocytopenia-absent-radius-syndrome/">Thrombocytopenia-absent radius syndrome</a></li>
|
||
|
||
|
||
<li>Tardive tibial muscular dystrophy, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/tibial-muscular-dystrophy/">Tibial muscular dystrophy</a></li>
|
||
|
||
|
||
<li><a href="https://medlineplus.gov/genetics/condition/tarsal-carpal-coalition-syndrome/">Tarsal-carpal coalition syndrome</a></li>
|
||
|
||
<li>Tarui disease, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/glycogen-storage-disease-type-vii/">Glycogen storage disease type VII</a></li>
|
||
|
||
|
||
<li>Task-specific dystonia, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/task-specific-focal-dystonia/">Task-specific focal dystonia</a></li>
|
||
|
||
|
||
<li><a href="https://medlineplus.gov/genetics/condition/task-specific-focal-dystonia/">Task-specific focal dystonia</a></li>
|
||
|
||
<li>Tatton-Brown-Rahman syndrome, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/dnmt3a-overgrowth-syndrome/">DNMT3A overgrowth syndrome</a></li>
|
||
|
||
|
||
<li><a href="https://medlineplus.gov/genetics/condition/tay-sachs-disease/">Tay-Sachs disease</a></li>
|
||
|
||
<li>Tay-Sachs disease, AB variant, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/gm2-activator-deficiency/">GM2 activator deficiency</a></li>
|
||
|
||
|
||
<li>Taybi syndrome, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/otopalatodigital-syndrome-type-1/">Otopalatodigital syndrome type 1</a></li>
|
||
|
||
|
||
<li>Taybi syndrome, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/otopalatodigital-syndrome-type-2/">Otopalatodigital syndrome type 2</a></li>
|
||
|
||
|
||
<li>TBG deficiency, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/inherited-thyroxine-binding-globulin-deficiency/">Inherited thyroxine-binding globulin deficiency</a></li>
|
||
|
||
|
||
<li>TBRS, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/dnmt3a-overgrowth-syndrome/">DNMT3A overgrowth syndrome</a></li>
|
||
|
||
|
||
<li>TC deficiency, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/transcobalamin-deficiency/">Transcobalamin deficiency</a></li>
|
||
|
||
|
||
<li>TC II deficiency, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/transcobalamin-deficiency/">Transcobalamin deficiency</a></li>
|
||
|
||
|
||
<li>TCC, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/tarsal-carpal-coalition-syndrome/">Tarsal-carpal coalition syndrome</a></li>
|
||
|
||
|
||
<li>TCD, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/choroideremia/">Choroideremia</a></li>
|
||
|
||
|
||
<li>TCN2 deficiency, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/transcobalamin-deficiency/">Transcobalamin deficiency</a></li>
|
||
|
||
|
||
<li>TD, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/tourette-syndrome/">Tourette syndrome</a></li>
|
||
|
||
|
||
<li>Telangiectasia, cerebello-oculocutaneous, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/ataxia-telangiectasia/">Ataxia-telangiectasia</a></li>
|
||
|
||
|
||
<li>Telomeric deletion 10, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/10q26-deletion-syndrome/">10q26 deletion syndrome</a></li>
|
||
|
||
|
||
<li>Telomeric deletion 17p, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/miller-dieker-syndrome/">Miller-Dieker syndrome</a></li>
|
||
|
||
|
||
<li>Terminal chromosome 10q26 deletion syndrome, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/10q26-deletion-syndrome/">10q26 deletion syndrome</a></li>
|
||
|
||
|
||
<li><a href="https://medlineplus.gov/genetics/condition/terminal-osseous-dysplasia/">Terminal osseous dysplasia</a></li>
|
||
|
||
<li>Terminal osseous dysplasia and pigmentary defect syndrome, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/terminal-osseous-dysplasia/">Terminal osseous dysplasia</a></li>
|
||
|
||
|
||
<li>Terminal osseous dysplasia and pigmentary defects, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/terminal-osseous-dysplasia/">Terminal osseous dysplasia</a></li>
|
||
|
||
|
||
<li>Terminal osseous dysplasia with pigmentary defects , <i>see</i> <a href="https://medlineplus.gov/genetics/condition/terminal-osseous-dysplasia/">Terminal osseous dysplasia</a></li>
|
||
|
||
|
||
<li>Terminal osseous dysplasia-pigmentary defects syndrome, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/terminal-osseous-dysplasia/">Terminal osseous dysplasia</a></li>
|
||
|
||
|
||
<li>Teschler-Nicola/Killian syndrome, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/pallister-killian-mosaic-syndrome/">Pallister-Killian mosaic syndrome</a></li>
|
||
|
||
|
||
<li>Testosterone 17-beta-dehydrogenase deficiency, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/17-beta-hydroxysteroid-dehydrogenase-3-deficiency/">17-beta hydroxysteroid dehydrogenase 3 deficiency</a></li>
|
||
|
||
|
||
<li>Testotoxicosis, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/familial-male-limited-precocious-puberty/">Familial male-limited precocious puberty</a></li>
|
||
|
||
|
||
<li>TETAMS, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/tetra-amelia-syndrome/">Tetra-amelia syndrome</a></li>
|
||
|
||
|
||
<li>Tetra-amelia, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/tetra-amelia-syndrome/">Tetra-amelia syndrome</a></li>
|
||
|
||
|
||
<li><a href="https://medlineplus.gov/genetics/condition/tetra-amelia-syndrome/">Tetra-amelia syndrome</a></li>
|
||
|
||
<li>Tetra-amelia, autosomal recessive, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/tetra-amelia-syndrome/">Tetra-amelia syndrome</a></li>
|
||
|
||
|
||
<li><a href="https://medlineplus.gov/genetics/condition/tetrahydrobiopterin-deficiency/">Tetrahydrobiopterin deficiency</a></li>
|
||
|
||
<li>Tetraphocomelia-cleft palate syndrome, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/roberts-syndrome/">Roberts syndrome</a></li>
|
||
|
||
|
||
<li>Tetrasomy 12p, mosaic, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/pallister-killian-mosaic-syndrome/">Pallister-Killian mosaic syndrome</a></li>
|
||
|
||
|
||
<li><a href="https://medlineplus.gov/genetics/condition/tetrasomy-18p/">Tetrasomy 18p</a></li>
|
||
|
||
<li>TFP deficiency, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/mitochondrial-trifunctional-protein-deficiency/">Mitochondrial trifunctional protein deficiency</a></li>
|
||
|
||
|
||
<li>TH deficiency, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/tyrosine-hydroxylase-deficiency/">Tyrosine hydroxylase deficiency</a></li>
|
||
|
||
|
||
<li>TH-deficient DRD, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/tyrosine-hydroxylase-deficiency/">Tyrosine hydroxylase deficiency</a></li>
|
||
|
||
|
||
<li>Thalassemia, beta type, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/beta-thalassemia/">Beta thalassemia</a></li>
|
||
|
||
|
||
<li>Thanatophoric dwarfism, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/thanatophoric-dysplasia/">Thanatophoric dysplasia</a></li>
|
||
|
||
|
||
<li><a href="https://medlineplus.gov/genetics/condition/thanatophoric-dysplasia/">Thanatophoric dysplasia</a></li>
|
||
|
||
<li>Thanatophoric short stature, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/thanatophoric-dysplasia/">Thanatophoric dysplasia</a></li>
|
||
|
||
|
||
<li>THAP1 dystonia, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/dystonia-6/">Dystonia 6</a></li>
|
||
|
||
|
||
<li>THE syndrome, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/trichohepatoenteric-syndrome/">Trichohepatoenteric syndrome</a></li>
|
||
|
||
|
||
<li>THES, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/trichohepatoenteric-syndrome/">Trichohepatoenteric syndrome</a></li>
|
||
|
||
|
||
<li>Thiamine metabolism dysfunction syndrome 2, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/biotin-thiamine-responsive-basal-ganglia-disease/">Biotin-thiamine-responsive basal ganglia disease</a></li>
|
||
|
||
|
||
<li>Thiamine transporter-2 deficiency, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/biotin-thiamine-responsive-basal-ganglia-disease/">Biotin-thiamine-responsive basal ganglia disease</a></li>
|
||
|
||
|
||
<li>Thiamine-responsive encephalopathy, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/biotin-thiamine-responsive-basal-ganglia-disease/">Biotin-thiamine-responsive basal ganglia disease</a></li>
|
||
|
||
|
||
<li><a href="https://medlineplus.gov/genetics/condition/thiamine-responsive-megaloblastic-anemia-syndrome/">Thiamine-responsive megaloblastic anemia syndrome</a></li>
|
||
|
||
<li>Thiamine-responsive megaloblastic anemia with diabetes mellitus and sensorineural hearing loss, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/thiamine-responsive-megaloblastic-anemia-syndrome/">Thiamine-responsive megaloblastic anemia syndrome</a></li>
|
||
|
||
|
||
<li>Thiopurine methyltransferase deficiency, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/thiopurine-s-methyltransferase-deficiency/">Thiopurine S-methyltransferase deficiency</a></li>
|
||
|
||
|
||
<li><a href="https://medlineplus.gov/genetics/condition/thiopurine-s-methyltransferase-deficiency/">Thiopurine S-methyltransferase deficiency</a></li>
|
||
|
||
<li>THMD2, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/biotin-thiamine-responsive-basal-ganglia-disease/">Biotin-thiamine-responsive basal ganglia disease</a></li>
|
||
|
||
|
||
<li>Thoracic aortic aneurysm, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/familial-thoracic-aortic-aneurysm-and-dissection/">Familial thoracic aortic aneurysm and dissection</a></li>
|
||
|
||
|
||
<li>Thoracic asphyxiant dystrophy, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/asphyxiating-thoracic-dystrophy/">Asphyxiating thoracic dystrophy</a></li>
|
||
|
||
|
||
<li>Thoracic-pelvic-phalangeal dystrophy, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/asphyxiating-thoracic-dystrophy/">Asphyxiating thoracic dystrophy</a></li>
|
||
|
||
|
||
<li>Three M syndrome, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/3-m-syndrome/">3-M syndrome</a></li>
|
||
|
||
|
||
<li>Three-M slender-boned nanism, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/3-m-syndrome/">3-M syndrome</a></li>
|
||
|
||
|
||
<li>Thrombocytopathy, asplenia, and miosis, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/stormorken-syndrome/">Stormorken syndrome</a></li>
|
||
|
||
|
||
<li>Thrombocytopenia 1, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/x-linked-thrombocytopenia/">X-linked thrombocytopenia</a></li>
|
||
|
||
|
||
<li>Thrombocytopenia absent radii, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/thrombocytopenia-absent-radius-syndrome/">Thrombocytopenia-absent radius syndrome</a></li>
|
||
|
||
|
||
<li><a href="https://medlineplus.gov/genetics/condition/thrombocytopenia-absent-radius-syndrome/">Thrombocytopenia-absent radius syndrome</a></li>
|
||
|
||
<li>Thrombophilia 1 due to thrombin defect, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/prothrombin-thrombophilia/">Prothrombin thrombophilia</a></li>
|
||
|
||
|
||
<li>Thrombophilia due to protein S deficiency, autosomal dominant, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/protein-s-deficiency/">Protein S deficiency</a></li>
|
||
|
||
|
||
<li>Thrombophilia due to protein S deficiency, autosomal recessive, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/protein-s-deficiency/">Protein S deficiency</a></li>
|
||
|
||
|
||
<li><a href="https://medlineplus.gov/genetics/condition/thrombotic-thrombocytopenic-purpura/">Thrombotic thrombocytopenic purpura</a></li>
|
||
|
||
<li>Thymidine phosphorylase deficiency, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/mitochondrial-neurogastrointestinal-encephalopathy-disease/">Mitochondrial neurogastrointestinal encephalopathy disease</a></li>
|
||
|
||
|
||
<li><a href="https://medlineplus.gov/genetics/condition/tibial-muscular-dystrophy/">Tibial muscular dystrophy</a></li>
|
||
|
||
<li>Tietz albinism-deafness syndrome, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/tietz-syndrome/">Tietz syndrome</a></li>
|
||
|
||
|
||
<li><a href="https://medlineplus.gov/genetics/condition/tietz-syndrome/">Tietz syndrome</a></li>
|
||
|
||
<li>Tietz's syndrome, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/tietz-syndrome/">Tietz syndrome</a></li>
|
||
|
||
|
||
<li><a href="https://medlineplus.gov/genetics/condition/timothy-syndrome/">Timothy syndrome</a></li>
|
||
|
||
<li>Titinopathy & early-onset myopathy with fatal cardiomyopathy, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/early-onset-myopathy-with-fatal-cardiomyopathy/">Early-onset myopathy with fatal cardiomyopathy</a></li>
|
||
|
||
|
||
<li>TK2-related mitochondrial DNA depletion myopathy, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/tk2-related-mitochondrial-dna-depletion-syndrome-myopathic-form/">TK2-related mitochondrial DNA depletion syndrome, myopathic form</a></li>
|
||
|
||
|
||
<li><a href="https://medlineplus.gov/genetics/condition/tk2-related-mitochondrial-dna-depletion-syndrome-myopathic-form/">TK2-related mitochondrial DNA depletion syndrome, myopathic form</a></li>
|
||
|
||
<li>TMAU, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/trimethylaminuria/">Trimethylaminuria</a></li>
|
||
|
||
|
||
<li>TMAuria, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/trimethylaminuria/">Trimethylaminuria</a></li>
|
||
|
||
|
||
<li>TMCO1 defect syndrome, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/cerebro-facio-thoracic-dysplasia/">Cerebro-facio-thoracic dysplasia</a></li>
|
||
|
||
|
||
<li>TMD, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/tibial-muscular-dystrophy/">Tibial muscular dystrophy</a></li>
|
||
|
||
|
||
<li>TNDM type 1, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/6q24-related-transient-neonatal-diabetes-mellitus/">6q24-related transient neonatal diabetes mellitus</a></li>
|
||
|
||
|
||
<li>TNF receptor-associated periodic fever syndrome, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/tumor-necrosis-factor-receptor-associated-periodic-syndrome/">Tumor necrosis factor receptor-associated periodic syndrome</a></li>
|
||
|
||
|
||
<li>TODPD, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/terminal-osseous-dysplasia/">Terminal osseous dysplasia</a></li>
|
||
|
||
|
||
<li>Tomaculous neuropathy, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/hereditary-neuropathy-with-liability-to-pressure-palsies/">Hereditary neuropathy with liability to pressure palsies</a></li>
|
||
|
||
|
||
<li>Torg syndrome, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/multicentric-osteolysis-nodulosis-and-arthropathy/">Multicentric osteolysis, nodulosis, and arthropathy</a></li>
|
||
|
||
|
||
<li>Torg-Winchester syndrome, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/multicentric-osteolysis-nodulosis-and-arthropathy/">Multicentric osteolysis, nodulosis, and arthropathy</a></li>
|
||
|
||
|
||
<li>Torsion dystonia 6, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/dystonia-6/">Dystonia 6</a></li>
|
||
|
||
|
||
<li>Torsion dystonia-parkinsonism, Filipino type, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/x-linked-dystonia-parkinsonism/">X-linked dystonia-parkinsonism</a></li>
|
||
|
||
|
||
<li>Total color blindness, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/achromatopsia/">Achromatopsia</a></li>
|
||
|
||
|
||
<li>Total hexosaminidase deficiency, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/sandhoff-disease/">Sandhoff disease</a></li>
|
||
|
||
|
||
<li>Total HPRT deficiency, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/lesch-nyhan-syndrome/">Lesch-Nyhan syndrome</a></li>
|
||
|
||
|
||
<li>Total hypotrichosis, Mari type, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/autosomal-recessive-hypotrichosis/">Autosomal recessive hypotrichosis</a></li>
|
||
|
||
|
||
<li>Total hypoxanthine-guanine phosphoribosyl transferase deficiency, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/lesch-nyhan-syndrome/">Lesch-Nyhan syndrome</a></li>
|
||
|
||
|
||
<li>Total lipodystrophy, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/congenital-generalized-lipodystrophy/">Congenital generalized lipodystrophy</a></li>
|
||
|
||
|
||
<li>Tourette disorder, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/tourette-syndrome/">Tourette syndrome</a></li>
|
||
|
||
|
||
<li><a href="https://medlineplus.gov/genetics/condition/tourette-syndrome/">Tourette syndrome</a></li>
|
||
|
||
<li>Tourette's disease, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/tourette-syndrome/">Tourette syndrome</a></li>
|
||
|
||
|
||
<li>Townes syndrome, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/townes-brocks-syndrome/">Townes-Brocks Syndrome</a></li>
|
||
|
||
|
||
<li><a href="https://medlineplus.gov/genetics/condition/townes-brocks-syndrome/">Townes-Brocks Syndrome</a></li>
|
||
|
||
<li>Toxemia of pregnancy, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/preeclampsia/">Preeclampsia</a></li>
|
||
|
||
|
||
<li>Toxic diffuse goiter, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/graves-disease/">Graves' disease</a></li>
|
||
|
||
|
||
<li>Toxic epidermal necrolysis, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/stevens-johnson-syndrome-toxic-epidermal-necrolysis/">Stevens-Johnson syndrome/toxic epidermal necrolysis</a></li>
|
||
|
||
|
||
<li>TPA deficiency, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/mitochondrial-trifunctional-protein-deficiency/">Mitochondrial trifunctional protein deficiency</a></li>
|
||
|
||
|
||
<li>TPI deficiency, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/triosephosphate-isomerase-deficiency/">Triosephosphate isomerase deficiency</a></li>
|
||
|
||
|
||
<li>TPID, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/triosephosphate-isomerase-deficiency/">Triosephosphate isomerase deficiency</a></li>
|
||
|
||
|
||
<li>TPMT deficiency, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/thiopurine-s-methyltransferase-deficiency/">Thiopurine S-methyltransferase deficiency</a></li>
|
||
|
||
|
||
<li><a href="https://medlineplus.gov/genetics/condition/transcobalamin-deficiency/">Transcobalamin deficiency</a></li>
|
||
|
||
<li>Transcobalamin II deficiency, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/transcobalamin-deficiency/">Transcobalamin deficiency</a></li>
|
||
|
||
|
||
<li>Transcortin deficiency, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/corticosteroid-binding-globulin-deficiency/">Corticosteroid-binding globulin deficiency</a></li>
|
||
|
||
|
||
<li>Transgrediens palmoplantar keratoderma of Siemens, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/mal-de-meleda/">Mal de Meleda</a></li>
|
||
|
||
|
||
<li>Transient neonatal diabetes mellitus 1, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/6q24-related-transient-neonatal-diabetes-mellitus/">6q24-related transient neonatal diabetes mellitus</a></li>
|
||
|
||
|
||
<li>Transmissible dementias, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/prion-disease/">Prion disease</a></li>
|
||
|
||
|
||
<li>Transmissible spongiform encephalopathies, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/prion-disease/">Prion disease</a></li>
|
||
|
||
|
||
<li><a href="https://medlineplus.gov/genetics/condition/transthyretin-amyloidosis/">Transthyretin amyloidosis</a></li>
|
||
|
||
<li>TRAPS, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/tumor-necrosis-factor-receptor-associated-periodic-syndrome/">Tumor necrosis factor receptor-associated periodic syndrome</a></li>
|
||
|
||
|
||
<li><a href="https://medlineplus.gov/genetics/condition/treacher-collins-syndrome/">Treacher Collins syndrome</a></li>
|
||
|
||
<li>Treacher Collins-Franceschetti syndrome, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/treacher-collins-syndrome/">Treacher Collins syndrome</a></li>
|
||
|
||
|
||
<li>Tremor-ataxia with central hypomyelination, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/pol-iii-related-leukodystrophy/">Pol III-related leukodystrophy</a></li>
|
||
|
||
|
||
<li>Tricho-hepato-enteric syndrome, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/trichohepatoenteric-syndrome/">Trichohepatoenteric syndrome</a></li>
|
||
|
||
|
||
<li>Tricho-rhino-phalangeal syndrome type II, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/trichorhinophalangeal-syndrome-type-ii/">Trichorhinophalangeal syndrome type II</a></li>
|
||
|
||
|
||
<li><a href="https://medlineplus.gov/genetics/condition/trichohepatoenteric-syndrome/">Trichohepatoenteric syndrome</a></li>
|
||
|
||
<li>Trichorhinophalangeal dysplasia type I, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/trichorhinophalangeal-syndrome-type-i/">Trichorhinophalangeal syndrome type I</a></li>
|
||
|
||
|
||
<li><a href="https://medlineplus.gov/genetics/condition/trichorhinophalangeal-syndrome-type-i/">Trichorhinophalangeal syndrome type I</a></li>
|
||
|
||
<li><a href="https://medlineplus.gov/genetics/condition/trichorhinophalangeal-syndrome-type-ii/">Trichorhinophalangeal syndrome type II</a></li>
|
||
|
||
<li>Trichorhinophalangeal syndrome with exostosis, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/trichorhinophalangeal-syndrome-type-ii/">Trichorhinophalangeal syndrome type II</a></li>
|
||
|
||
|
||
<li><a href="https://medlineplus.gov/genetics/condition/trichothiodystrophy/">Trichothiodystrophy</a></li>
|
||
|
||
<li>Trifunctional protein deficiency, type 1, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/long-chain-3-hydroxyacyl-coa-dehydrogenase-deficiency/">Long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency</a></li>
|
||
|
||
|
||
<li>Trifunctional protein deficiency, type 2, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/mitochondrial-trifunctional-protein-deficiency/">Mitochondrial trifunctional protein deficiency</a></li>
|
||
|
||
|
||
<li>Triglyceride storage disease with ichthyosis, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/chanarin-dorfman-syndrome/">Chanarin-Dorfman syndrome</a></li>
|
||
|
||
|
||
<li>Triglyceride storage disease with impaired long-chain fatty acid oxidation, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/chanarin-dorfman-syndrome/">Chanarin-Dorfman syndrome</a></li>
|
||
|
||
|
||
<li><a href="https://medlineplus.gov/genetics/condition/trimethylaminuria/">Trimethylaminuria</a></li>
|
||
|
||
<li>Triose phosphate isomerase deficiency, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/triosephosphate-isomerase-deficiency/">Triosephosphate isomerase deficiency</a></li>
|
||
|
||
|
||
<li><a href="https://medlineplus.gov/genetics/condition/triosephosphate-isomerase-deficiency/">Triosephosphate isomerase deficiency</a></li>
|
||
|
||
<li><a href="https://medlineplus.gov/genetics/condition/triple-a-syndrome/">Triple A syndrome</a></li>
|
||
|
||
<li>Triple H syndrome, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/ornithine-translocase-deficiency/">Ornithine translocase deficiency</a></li>
|
||
|
||
|
||
<li>Triple symptom complex, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/behcet-disease/">Behçet disease</a></li>
|
||
|
||
|
||
<li>Triple X syndrome, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/trisomy-x/">Trisomy X</a></li>
|
||
|
||
|
||
<li>Triplo X syndrome, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/trisomy-x/">Trisomy X</a></li>
|
||
|
||
|
||
<li><a href="https://medlineplus.gov/genetics/condition/trisomy-13/">Trisomy 13</a></li>
|
||
|
||
<li>Trisomy 13 syndrome, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/trisomy-13/">Trisomy 13</a></li>
|
||
|
||
|
||
<li><a href="https://medlineplus.gov/genetics/condition/trisomy-18/">Trisomy 18</a></li>
|
||
|
||
<li>Trisomy 18 syndrome, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/trisomy-18/">Trisomy 18</a></li>
|
||
|
||
|
||
<li>Trisomy 21, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/down-syndrome/">Down syndrome</a></li>
|
||
|
||
|
||
<li>Trisomy 3q29, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/3q29-microduplication-syndrome/">3q29 microduplication syndrome</a></li>
|
||
|
||
|
||
<li>Trisomy 7q11.23, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/7q1123-duplication-syndrome/">7q11.23 duplication syndrome</a></li>
|
||
|
||
|
||
<li>Trisomy E syndrome, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/trisomy-18/">Trisomy 18</a></li>
|
||
|
||
|
||
<li>Trisomy G, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/down-syndrome/">Down syndrome</a></li>
|
||
|
||
|
||
<li><a href="https://medlineplus.gov/genetics/condition/trisomy-x/">Trisomy X</a></li>
|
||
|
||
<li>Trisomy X, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/trisomy-x/">Trisomy X</a></li>
|
||
|
||
|
||
<li>Trisomy Xq28, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/mecp2-duplication-syndrome/">MECP2 duplication syndrome</a></li>
|
||
|
||
|
||
<li>TRMA, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/thiamine-responsive-megaloblastic-anemia-syndrome/">Thiamine-responsive megaloblastic anemia syndrome</a></li>
|
||
|
||
|
||
<li><a href="https://medlineplus.gov/genetics/condition/trnt1-deficiency/">TRNT1 deficiency</a></li>
|
||
|
||
<li>TRNT1 enzyme deficiency, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/trnt1-deficiency/">TRNT1 deficiency</a></li>
|
||
|
||
|
||
<li>TRNT1-related immunodeficiency, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/trnt1-deficiency/">TRNT1 deficiency</a></li>
|
||
|
||
|
||
<li>TRNT1-related immunodeficiency+, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/trnt1-deficiency/">TRNT1 deficiency</a></li>
|
||
|
||
|
||
<li>Troisier-Hanot-Chauffard syndrome, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/hereditary-hemochromatosis/">Hereditary hemochromatosis</a></li>
|
||
|
||
|
||
<li><a href="https://medlineplus.gov/genetics/condition/troyer-syndrome/">Troyer syndrome</a></li>
|
||
|
||
<li>TRP syndrome, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/trichorhinophalangeal-syndrome-type-i/">Trichorhinophalangeal syndrome type I</a></li>
|
||
|
||
|
||
<li>TRPS I, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/trichorhinophalangeal-syndrome-type-i/">Trichorhinophalangeal syndrome type I</a></li>
|
||
|
||
|
||
<li>TRPS II, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/trichorhinophalangeal-syndrome-type-ii/">Trichorhinophalangeal syndrome type II</a></li>
|
||
|
||
|
||
<li>TRPS1, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/trichorhinophalangeal-syndrome-type-i/">Trichorhinophalangeal syndrome type I</a></li>
|
||
|
||
|
||
<li>TRPS2, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/trichorhinophalangeal-syndrome-type-ii/">Trichorhinophalangeal syndrome type II</a></li>
|
||
|
||
|
||
<li>True microcephaly, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/autosomal-recessive-primary-microcephaly/">Autosomal recessive primary microcephaly</a></li>
|
||
|
||
|
||
<li>TS, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/turner-syndrome/">Turner syndrome</a></li>
|
||
|
||
|
||
<li>TS, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/tourette-syndrome/">Tourette syndrome</a></li>
|
||
|
||
|
||
<li>TS, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/timothy-syndrome/">Timothy syndrome</a></li>
|
||
|
||
|
||
<li>TSD, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/tay-sachs-disease/">Tay-Sachs disease</a></li>
|
||
|
||
|
||
<li>TSEs, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/prion-disease/">Prion disease</a></li>
|
||
|
||
|
||
<li>TTD, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/trichothiodystrophy/">Trichothiodystrophy</a></li>
|
||
|
||
|
||
<li>TTP, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/thrombotic-thrombocytopenic-purpura/">Thrombotic thrombocytopenic purpura</a></li>
|
||
|
||
|
||
<li>TUBB4A-associated hypomyelinating leukoencephalopathies, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/tubb4a-related-leukodystrophy/">TUBB4A-related leukodystrophy</a></li>
|
||
|
||
|
||
<li>TUBB4A-related hypomyelinating leukodystrophy, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/tubb4a-related-leukodystrophy/">TUBB4A-related leukodystrophy</a></li>
|
||
|
||
|
||
<li><a href="https://medlineplus.gov/genetics/condition/tubb4a-related-leukodystrophy/">TUBB4A-related leukodystrophy</a></li>
|
||
|
||
<li>Tuberose sclerosis, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/tuberous-sclerosis-complex/">Tuberous sclerosis complex</a></li>
|
||
|
||
|
||
<li><a href="https://medlineplus.gov/genetics/condition/tuberous-sclerosis-complex/">Tuberous sclerosis complex</a></li>
|
||
|
||
<li><a href="https://medlineplus.gov/genetics/condition/tubular-aggregate-myopathy/">Tubular aggregate myopathy</a></li>
|
||
|
||
<li>Tubular hypomagnesemia-hypokalemia with hypocalcuria, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/gitelman-syndrome/">Gitelman syndrome</a></li>
|
||
|
||
|
||
<li><a href="https://medlineplus.gov/genetics/condition/tumor-necrosis-factor-receptor-associated-periodic-syndrome/">Tumor necrosis factor receptor-associated periodic syndrome</a></li>
|
||
|
||
<li>Tumor of the Ewing family, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/ewing-sarcoma/">Ewing sarcoma</a></li>
|
||
|
||
|
||
<li>Tumor of the urinary bladder, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/bladder-cancer/">Bladder cancer</a></li>
|
||
|
||
|
||
<li>Tumor, Wilms, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/wilms-tumor/">Wilms tumor</a></li>
|
||
|
||
|
||
<li>Turner phenotype with normal karyotype, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/noonan-syndrome/">Noonan syndrome</a></li>
|
||
|
||
|
||
<li><a href="https://medlineplus.gov/genetics/condition/turner-syndrome/">Turner syndrome</a></li>
|
||
|
||
<li>Turner syndrome in female with X chromosome, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/noonan-syndrome/">Noonan syndrome</a></li>
|
||
|
||
|
||
<li>Turner's syndrome, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/turner-syndrome/">Turner syndrome</a></li>
|
||
|
||
|
||
<li>Turner-Kieser syndrome, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/nail-patella-syndrome/">Nail-patella syndrome</a></li>
|
||
|
||
|
||
<li>Turner-like syndrome, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/noonan-syndrome/">Noonan syndrome</a></li>
|
||
|
||
|
||
<li><a href="https://medlineplus.gov/genetics/condition/type-1-diabetes/">Type 1 diabetes</a></li>
|
||
|
||
<li>Type 1 diabetes mellitus, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/type-1-diabetes/">Type 1 diabetes</a></li>
|
||
|
||
|
||
<li>Type 1 lissencephaly, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/isolated-lissencephaly-sequence/">Isolated lissencephaly sequence</a></li>
|
||
|
||
|
||
<li>Type 1 spinocerebellar ataxia, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/spinocerebellar-ataxia-type-1/">Spinocerebellar ataxia type 1</a></li>
|
||
|
||
|
||
<li><a href="https://medlineplus.gov/genetics/condition/type-2-diabetes/">Type 2 diabetes</a></li>
|
||
|
||
<li>Type 2 diabetes mellitus, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/type-2-diabetes/">Type 2 diabetes</a></li>
|
||
|
||
|
||
<li>Type 6 spinocerebellar ataxia, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/spinocerebellar-ataxia-type-6/">Spinocerebellar ataxia type 6</a></li>
|
||
|
||
|
||
<li>Type A insulin resistance, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/type-a-insulin-resistance-syndrome/">Type A insulin resistance syndrome</a></li>
|
||
|
||
|
||
<li><a href="https://medlineplus.gov/genetics/condition/type-a-insulin-resistance-syndrome/">Type A insulin resistance syndrome</a></li>
|
||
|
||
<li>Type I acrocephalosyndactyly, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/apert-syndrome/">Apert syndrome</a></li>
|
||
|
||
|
||
<li>Type I familial amyloid polyneuropathy, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/transthyretin-amyloidosis/">Transthyretin amyloidosis</a></li>
|
||
|
||
|
||
<li>Type II 3β-hydroxysteroid dehydrogenase deficiency, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/3-beta-hydroxysteroid-dehydrogenase-deficiency/">3-beta-hydroxysteroid dehydrogenase deficiency</a></li>
|
||
|
||
|
||
<li>Type II acrocephalosyndactyly, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/carpenter-syndrome/">Carpenter syndrome</a></li>
|
||
|
||
|
||
<li>Type II ataxia with lactic acidosis, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/pyruvate-carboxylase-deficiency/">Pyruvate carboxylase deficiency</a></li>
|
||
|
||
|
||
<li>Type II familial amyloid polyneuropathy, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/transthyretin-amyloidosis/">Transthyretin amyloidosis</a></li>
|
||
|
||
|
||
<li>Type IV glycogenosis, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/glycogen-storage-disease-type-iv/">Glycogen storage disease type IV</a></li>
|
||
|
||
|
||
<li>Typus degenerativus amstelodamensis, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/cornelia-de-lange-syndrome/">Cornelia de Lange syndrome</a></li>
|
||
|
||
|
||
<li>Tyrosinaemia, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/tyrosinemia/">Tyrosinemia</a></li>
|
||
|
||
|
||
<li><a href="https://medlineplus.gov/genetics/condition/tyrosine-hydroxylase-deficiency/">Tyrosine hydroxylase deficiency</a></li>
|
||
|
||
<li>Tyrosine hydroxylase-deficient dopa-responsive dystonia, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/tyrosine-hydroxylase-deficiency/">Tyrosine hydroxylase deficiency</a></li>
|
||
|
||
|
||
<li><a href="https://medlineplus.gov/genetics/condition/tyrosinemia/">Tyrosinemia</a></li>
|
||
|
||
</ul>
|
||
|
||
</section>
|
||
|
||
<section>
|
||
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|
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|
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</section>
|
||
|
||
</div>
|
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</article>
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