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
07072 ATFB8 fibrillation, atrial, familial, type 8, susceptibility to 613055 AD - - ZFHX3 - -
01524 cancer, prostate cancer, prostate 176807 AD;SMu 252 204 AR, BRCA2, CD82, CDH1, CHEK2, HIP1, KLF6, MAD1L1, MSR1, MXI1, PTEN, ZFHX3 - -
05611 NDD neurodevelopmental disorder (NDD) - - 3873 3688 ACBD6, ADARB1, AP1G1, ARFGEF1, ATP9A, CAMSAP1, CAPRIN1, CASP2, CHASERR, CLCN3, CPSF3L, DDB1, DENND5B, DHX30, DHX9, DOHH, DOT1L, EEFSEC, EIF2C1, EIF2C2, 79 more - -
07071 SCA4 ataxia, spinocerebellar, type 4 600223 AD - - ZFHX3 - -
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