All diseases

5 entries on 1 page. Showing entries 1 - 5.
Legend   How to query  

ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
02627 - 46,XY gonadal dysgenesis, partial, with minifascicular neuropathy 607080 - 7 7 DHH - -
00139 ID intellectual disability (ID) - - 1837 1570 AAAS, AARS2, ABCD1, ABCD4, ABHD5, ACAD9, ACO2, ACOX1, ACSF3, ACSL4, ACTB, ACTG1, ADAMTS10, ADAR, ADCK3, ADSL, AFF2, AGA, AGTR2, AHI1, 536 more - -
00830 MRX91 mental retardation, X-linked, type 91 (MRX91) 300577 XLD 0 0 ZDHHC15 - -
00838 MRXSR mental retardation, X-linked syndromic, Raymond type (MRXSR) 300799 - 1 1 ZDHHC9 - -
01828 SRXY-7 46,XY sex reversal, type 7 (SRXY-7) 233420 - 0 0 DHH - -
Legend   How to query