All diseases

4 entries on 1 page. Showing entries 1 - 4.
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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
00139 ID intellectual disability (ID) - - 2794 2475 AAAS, AARS2, ABCD1, ABCD4, ABHD5, ACAD9, ACO2, ACOX1, ACSF3, ACSL4, ACTB, ACTG1, ADAMTS10, ADAR, ADCK3, ADSL, AFF2, AGA, AGTR2, AHI1, 556 more - -
07015 MARTS Martsolf syndrome - - - - RAB3GAP1, RAB3GAP2 - -
00560 MARTS1 Martsolf syndrome, type 1 212720 AR 3 3 RAB3GAP2 - -
00094 WARBM2 Warburg micro syndrome, type 2 (WARBM2) 614225 AR 1 2 RAB3GAP2 - -
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