All diseases

4 entries on 1 page. Showing entries 1 - 4.
Legend   How to query  

ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
00811 - atrophy, muscular, spinal, lower extremity, autosomal dominant 158600 - - - DYNC1H1 - -
00809 CMT-2O Charcot-Marie-Tooth disease, axonal, type 2O (CMT-2O) 614228 - - - DYNC1H1 - -
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 - -
00810 MRD-13 mental retardation, autosomal dominant, type 13 (MRD-13) 614563 - - - DYNC1H1 - -
Legend   How to query