All diseases

10 entries on 1 page. Showing entries 1 - 10.
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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
05232 APA adenoma, adrenal aldosterone-producing (APA) - - 5 5 CACNA1D, CTNNB1, KCNJ5 - -
01221 cancer, liver cancer, hepatocellular (HCC) 114550 - 4 4 APC, AXIN1, CASP8, CTNNB1, IGF2R, MET, PDGFRL, PIK3CA, TP53 liver -
00424 cancer, ovarian cancer, ovarian 167000 - 231 165 AKT1, CDH1, CTNNB1, OPCML, PARK2, PIK3CA - -
00091 CRC cancer, colorectal, susceptibility to (CRC) 114500 AD;SMu 3056 1829 AKT1, APC, AURKA, AXIN2, BAX, BUB1B, CCND1, CTNNB1, DCC, DLC1, EP300, FGFR3, FLCN, MCC, MLH3, NRAS, NTHL1, ODC1, PDGFRL, PIK3CA, 7 more - -
05636 EVR7 vitreoretinopathy exudative, type 7 (EVR-7) 617572 AD 8 8 CTNNB1 - -
04240 EVR;FEVR vitreoretinopathy, exudative (EVR; familial FVER)) - - 243 218 CTNNB1, FZD4, LRP5, NDP, TSPAN12, ZNF408 - -
00139 ID intellectual disability (ID) - - 2195 1894 AAAS, AARS2, ABCD1, ABCD4, ABHD5, ACAD9, ACO2, ACOX1, ACSF3, ACSL4, ACTB, ACTG1, ADAMTS10, ADAR, ADCK3, ADSL, AFF2, AGA, AGTR2, AHI1, 540 more - -
01429 MDB medulloblastoma (MDB) 155255 - 9 7 BRCA2, CTNNB1, PTCH2, SUFU - -
03823 NEDSDV;MRD19 eurodevelopmental disorder with spastic diplegia and visual defects (NEDSDV, MRD19) 615075 AD 3 3 CTNNB1 - -
01317 PILOMATRICOMA pilomatrixoma 132600 - 0 0 CTNNB1, MUTYH - -
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