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
00683 - cancer, breast, familial 114480 - 8012 749 AKT1, ATM, BARD1, BRCA1, BRCA2, BRIP1, CASP8, CDH1, CHEK2, ESR1, HMMR, KRAS, NQO2, PALB2, PHB, PIK3CA, PPM1D, RAD51, RAD54L, RB1CC1, 4 more - -
00424 cancer, ovarian cancer, ovarian 167000 - 216 151 AKT1, CDH1, CTNNB1, OPCML, PARK2, PIK3CA - -
00091 CRC cancer, colorectal (CRC) 114500 - 2940 1714 AKT1, APC, AURKA, AXIN2, BAX, BUB1B, CCND1, CTNNB1, DCC, DLC1, EP300, FGFR3, FLCN, MCC, MLH3, NRAS, NTHL1, ODC1, PDGFRL, PIK3CA, 7 more - -
03832 CWS-6 Cowden syndrome, type 6 (CWS-6) 615109 - 0 0 AKT1 - -
01526 Proteus syndrome, Proteus, somatic 176920 - 0 0 AKT1 - -
00212 SCZD schizophrenia (SCZD) 181500 - 51 49 AKT1, APOL2, APOL4, CHI3L1, COMT, DAO, DAOA, DISC1, DISC2, DRD3, DTNBP1, HTR2A, MTHFR, RTN4R - -
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