All diseases

13 entries on 1 page. Showing entries 1 - 13.
Legend   How to query  

ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
00600 - nevus, epidermal 162900 - 1 1 FGFR3, HRAS, NRAS, PIK3CA - -
01556 - keratosis, seborrheic 182000 - 0 0 PIK3CA - -
00683 cancer, breast cancer, breast, susceptibility 114480 - 8102 785 AKT1, ATM, BARD1, BRCA1, BRCA2, BRIP1, CASP8, CDH1, CHEK2, ESR1, HMMR, KRAS, NQO2, PALB2, PHB, PIK3CA, PPM1D, RAD51, RAD54L, RB1CC1, 4 more - -
03381 cancer, gastric cancer, gastric (Neoplasm of stomach) 613659 - 97 83 APC, CASP10, ERBB2, FGFR2, IRF1, KLF6, MUTYH, PIK3CA - -
01221 cancer, liver cancer, hepatocellular (HCC) 114550 - 4 4 APC, AXIN1, CASP8, CTNNB1, IGF2R, MET, PDGFRL, PIK3CA, TP53 liver -
00639 cancer, lung cancer, lung (adenocarcinoma) 211980 - 52 40 BRAF, CASP8, CYP2A6, DLEC1, EGFR, ERBB2, ERCC6, FASLG, IRF1, KRAS, MAP3K8, PARK2, PIK3CA, PPP2R1B, RASSF1, SFTPA2, SLC22A18 - -
00424 cancer, ovarian cancer, ovarian 167000 - 231 165 AKT1, CDH1, CTNNB1, OPCML, PARK2, PIK3CA - -
06553 CLAPO CLAPO syndrome, somatic 613089 - 0 0 PIK3CA - -
03203 CLOVE CLOVE syndrome, somatic (CLOVE, overgrowth, lipomatous, congenital, vascular malformations, and epidermal nevi) 612918 - 0 0 PIK3CA - -
00091 CRC cancer, colorectal, susceptibility to (CRC) 114500 AD;SMu 3059 1832 AKT1, APC, AURKA, AXIN2, BAX, BUB1B, CCND1, CTNNB1, DCC, DLC1, EP300, FGFR3, FLCN, MCC, MLH3, NRAS, NTHL1, ODC1, PDGFRL, PIK3CA, 7 more - -
03831 CWS5 Cowden syndrome, type 5 (CWS-5) 615108 - 0 0 PIK3CA - -
00382 MCAP megalencephaly-capillary malformation-polymicrogyria syndrome, somatic (MCAP) 602501 - 2 2 PIK3CA - -
06548 MEGALODACTYLY Macrodactyly, somatic 155500 - 0 0 PIK3CA - -
Legend   How to query