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) - - 1787 1520 AAAS, AARS2, ABCD1, ABCD4, ABHD5, ACAD9, ACO2, ACOX1, ACSF3, ACSL4, ACTB, ACTG1, ADAMTS10, ADAR, ADCK3, ADSL, AFF2, AGA, AGTR2, AHI1, 535 more - -
00759 NBIA-2A neurodegeneration, with brain iron accumulation, type 2A (NBIA-2A, infantile neuroaxonal dystrophy, type 1) 256600 - 6 6 PLA2G6 - -
00760 NBIA-2B neurodegeneration, with brain iron accumulation, type 2B (NBIA-2B) 610217 - 1 1 PLA2G6 - -
00761 PARK-14 Parkinson disease, type 14 (PARK-14) 612953 - 4 3 PLA2G6 - -
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