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
03079 COQ10D-4;SCAR-9 coenzyme Q10 deficiency, primary, type 4 (COQ10D-4, spinocerebellar ataxia, autosomal recessive, type 9 (SCAR-9)) 612016 - - - ADCK3 - -
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 - -
04200 SCAR-9 ataxia, spinocerebellar, autosomal recessive, type 9 (SCAR-9, coenzyme Q10 deficiency, primary, type 4 (COQ10D-4)) - - - - ADCK3 - -
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