Disease #00091 (CRC (cancer, colorectal, susceptibility to (CRC)), OMIM:114500)
Official abbreviation |
CRC |
Name |
cancer, colorectal, susceptibility to (CRC) |
OMIM ID |
114500 |
Human Phenotype Ontology Project (HPO) |
HPO |
Inheritance |
Autosomal dominant, Somatic mutation |
Individuals reported having this disease |
3060 |
Phenotype entries for this disease |
1833 |
Associated with 27 genes |
AKT1, APC, AURKA, AXIN2, BAX, BUB1B, CCND1, CTNNB1, DCC, DLC1, EP300, FGFR3, FLCN, MCC, MLH3, NRAS, NTHL1, ODC1, PDGFRL, PIK3CA, 7 more...AKT1, APC, AURKA, AXIN2, BAX, BUB1B, CCND1, CTNNB1, DCC, DLC1, EP300, FGFR3, FLCN, MCC, MLH3, NRAS, NTHL1, ODC1, PDGFRL, PIK3CA, PLA2G2A, PTPN12, PTPRJ, RAD54B, TLR2, TLR4, TP53 |
Associated tissues |
- |
Disease features |
- |
Remarks |
- |
Date created |
2012-12-07 10:49:46 +01:00 (CET) |
Date last edited |
2021-12-10 21:51:32 +01:00 (CET) |
Individuals
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