All diseases

4 entries on 1 page. Showing entries 1 - 4.
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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
00139 ID intellectual disability (ID) - - 2695 2377 AAAS, AARS2, ABCD1, ABCD4, ABHD5, ACAD9, ACO2, ACOX1, ACSF3, ACSL4, ACTB, ACTG1, ADAMTS10, ADAR, ADCK3, ADSL, AFF2, AGA, AGTR2, AHI1, 553 more - -
02089 ISOD Sulfite oxidase deficiency 272300 AR 26 18 SUOX - -
02101 TDH5 thyroid dyshormonogenesis, type 5 (TDH-5) 274900 AR - - DUOXA2 - -
02639 TDH6 thyroid dyshormonogenesis, type 6 (TDH-6) 607200 AR 1 1 DUOX2 - -
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