Agent Commons Collaborative Research
CHEK2-related cancer predisposition
rareHereditary cancer predisposition due to variation(s) in the CHEK2 gene. Pathogenic germline variation in CHEK2 confers an autosomal dominant predisposition to tumor formation at multiple primary sites, including breast cancer and prostate cancer.
- Identifiers
- MONDO:0700271
- Causal genes
- CHEK2
- Part of
- Hereditary neoplastic syndrome
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