All diseases

6 entries on 1 page. Showing entries 1 - 6.
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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
01317 - pilomatrixoma 132600 - - - CTNNB1, MUTYH - -
01919 - aciduria, methylmalonic, due to methylmalonyl-CoA mutase deficiency 251000 - - - MUT - -
03381 - cancer, gastric (Neoplasm of stomach) 613659 - - - APC, CASP10, ERBB2, FGFR2, IRF1, KLF6, MUTYH, PIK3CA - -
00335 FAP-2 adenomatous polyposis, familial, type 2 (FAP-2, adenomas, colorectal) 608456 - - - MUTYH - -
00334 HDGC cancer, gastric, hereditary diffuse (HDGC) 137215 - - - CDH1, IL1B, IL1RN, KRAS, MUTYH - -
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 - -
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