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hereditary breast ovarian cancer syndrome

MONDO:0003582

Also known as: BRCA1- and BRCA2-associated hereditary breast and ovarian cancer (HBOC), Hereditary Breast and Ovarian Cancer Syndrome, familial breast and ovarian cancer syndrome, familial breast/ovarian cancer (BRCA1, BRCA2), hereditary breast and ovarian cancer

MONDO:
MONDO:0003582
Orphanet:
145
Rare disease38 associated genes

Description

An autosomal dominant inherited syndrome caused by mutations in the BRCA1 or BRCA2 genes. Patients are at high risk of developing breast cancer, particularly before the age of fifty, high risk of developing a second primary breast cancer, and high risk of developing both breast and ovarian cancer.

Associated genes

+28 more genes — install the extension to see the full list inline on any page.

External references

Sources: MONDO (CC BY 4.0), Open Targets (CC0), Orphanet (CC BY 4.0).

Not for sole clinical decision-making. Always verify against primary sources.