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) - - 2210 1907 AAAS, AARS2, ABCD1, ABCD4, ABHD5, ACAD9, ACO2, ACOX1, ACSF3, ACSL4, ACTB, ACTG1, ADAMTS10, ADAR, ADCK3, ADSL, AFF2, AGA, AGTR2, AHI1, 542 more - -
00623 MEGDEL 3-methylglutaconic aciduria with deafness, encephalopathy, Leigh-like syndrome (MEGDEL) 614739 AR 16 16 SERAC1 - -
06748 MRD48 Mental retardation, autosomal dominant 48 617751 AD 0 0 RAC1 - -
Legend   How to query