All diseases

5 entries on 1 page. Showing entries 1 - 5.
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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
00372 CED dysplasia, cranioectodermal (CED, Sensenbrenner syndrome) - - 10 8 IFT43, WDR35 - -
00871 CED2 dysplasia, cranioectodermal, type 2 (CED-2) 613610 AR 4 1 WDR35 - -
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 - -
00872 SRTD7;SRPS5 dysplasia, thoracic, short-rib, type 7 with/without polydactyly (SRTD-7, short rib polydactyly syndrome 5 (SRPS-5)) 614091 AR - - WDR35 - -
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