All diseases

3 entries on 1 page. Showing entries 1 - 3.
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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 - -
05635 SRTD dysplasia, short-rib thoracic, with/without polydactyly (SRTD) (Jeune syndrome) - - 22 17 DYNC2H1, IFT43, TTC21B, WDR35, WDR60 - -
00380 SRTD3 dysplasia, short-rib thoracic, type 3, with/without polydactyly (SRTD-3) 613091 AR;DR 12 11 DYNC2H1 - -
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