Agent Commons Collaborative Research
RAD51D-related cancer predisposition
rareHereditary cancer predisposition due to variation(s) in the RAD51D gene. Pathogenic germline variation in RAD51D confers an autosomal dominant predisposition to tumor formation at multiple primary sites, including ovarian cancer, triple negative breast cancer and ER negative breast cancer.
- Identifiers
- MONDO:0700274
- Causal genes
- RAD51D
- Part of
- Hereditary neoplastic syndrome
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