All diseases

3 entries on 1 page. Showing entries 1 - 3.
Legend   How to query  

ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
00139 ID intellectual disability (ID) - - - - AAAS, AARS2, ABCD1, ABCD4, ABHD5, ACAD9, ACO2, ACOX1, ACSF3, ACSL4, ACTB, ACTG1, ADAMTS10, ADAR, ADCK3, ADSL, AFF2, AGA, AGTR2, AHI1, 515 more - -
00380 SRTD-3;SRPS-2B dysplasia, thoracic, short-rib, type 3 with or without polydactyly (SRTD-3, short rib polydactyly syndrome 2B (SRPS-2B)) 613091 - - - DYNC2H1 - -
00677 SRTD-6;SRPS-2A dysplasia, thoracic, short-rib, type 6 with or without polydactyly (SRTD-6, short rib polydactyly syndrome 2A (SRPS-2A)) 263520 - - - DYNC2H1, NEK1 - -
Legend   How to query