All diseases

3 entries on 1 page. Showing entries 1 - 3.
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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
00327 COQ10D1 coenzyme Q10 deficiency, primary, type 1 (COQ10D-1) 607426 AR - - COQ2 - -
00139 ID intellectual disability (ID) - - 2708 2390 AAAS, AARS2, ABCD1, ABCD4, ABHD5, ACAD9, ACO2, ACOX1, ACSF3, ACSL4, ACTB, ACTG1, ADAMTS10, ADAR, ADCK3, ADSL, AFF2, AGA, AGTR2, AHI1, 554 more - -
01391 MSA1 multisystem atrophy, susc.to, type 1 (MSA-1, Shy-Drager syndrome) 146500 AD;AR - - COQ2 - -
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