All diseases

11 entries on 1 page. Showing entries 1 - 11.
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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
00600 - nevus, epidermal 162900 - 0 0 FGFR3, HRAS, NRAS, PIK3CA - -
00683 - cancer, breast, familial 114480 - 8100 783 AKT1, ATM, BARD1, BRCA1, BRCA2, BRIP1, CASP8, CDH1, CHEK2, ESR1, HMMR, KRAS, NQO2, PALB2, PHB, PIK3CA, PPM1D, RAD51, RAD54L, RB1CC1, 4 more - -
01556 - keratosis, seborrheic 182000 - 0 0 PIK3CA - -
00639 ACLC cancer, lung (adenocarcinoma) 211980 - 11 8 BRAF, CASP8, CYP2A6, DLEC1, EGFR, ERBB2, ERCC6, FASLG, IRF1, KRAS, MAP3K8, PARK2, PIK3CA, PPP2R1B, RASSF1, SFTPA2, SLC22A18 - -
03381 cancer, gastric cancer, gastric (Neoplasm of stomach) 613659 - 93 79 APC, CASP10, ERBB2, FGFR2, IRF1, KLF6, MUTYH, PIK3CA - -
01221 cancer, liver cancer, hepatocellular 114550 - 4 4 APC, AXIN1, CASP8, CTNNB1, IGF2R, MET, PDGFRL, PIK3CA, TP53 liver -
00424 cancer, ovarian cancer, ovarian 167000 - 220 155 AKT1, CDH1, CTNNB1, OPCML, PARK2, PIK3CA - -
03203 CLOVE CLOVE syndrome, somatic (CLOVE, overgrowth, lipomatous, congenital, vascular malformations, and epidermal nevi) 612918 - 0 0 PIK3CA - -
00091 CRC cancer, colorectal (CRC) 114500 - 2966 1739 AKT1, APC, AURKA, AXIN2, BAX, BUB1B, CCND1, CTNNB1, DCC, DLC1, EP300, FGFR3, FLCN, MCC, MLH3, NRAS, NTHL1, ODC1, PDGFRL, PIK3CA, 7 more - -
03831 CWS-5 Cowden syndrome, type 5 (CWS-5) 615108 - 0 0 PIK3CA - -
00382 MCAP megalencephaly-capillary malformation-polymicrogyria syndrome, somatic (MCAP) 602501 - 2 2 PIK3CA - -
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