All diseases

2 entries on 1 page. Showing entries 1 - 2.
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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
00489 HPS-7 Hermansky-Pudlak syndrome, type 7 (HPS-7) 614076 - - - DTNBP1 - -
00212 SCZD schizophrenia (SCZD) 181500 - - - AKT1, APOL2, APOL4, CHI3L1, COMT, DAO, DAOA, DISC1, DISC2, DRD3, DTNBP1, HTR2A, MTHFR, RTN4R - -
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