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
04352 COWCK Cowchock syndrome (COWCK) 310490 - 0 0 AIFM1 - -
04351 COXPD-6 oxidative phosphorylation deficiency, combined, type 6 (COXPD-6) 300816 - 0 0 AIFM1 - -
00139 ID intellectual disability (ID) - - 1139 1015 AAAS, AARS2, ABCD1, ABCD4, ABHD5, ACAD9, ACO2, ACOX1, ACSF3, ACSL4, ACTB, ACTG1, ADAMTS10, ADAR, ADCK3, ADSL, AFF2, AGA, AGTR2, AHI1, 524 more - -
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