hereditary breast ovarian cancer syndrome
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. [ NCIT:C8493 ]
Term info
- GARD:0012352 (MONDO:equivalentTo)
- ICD10CM:C50 (Orphanet:145/nd)
- UMLS:C0677776 (Orphanet:145/e)
- DOID:5683 (MONDO:equivalentTo)
- OMIMPS:604370 (MONDO:equivalentTo)
- Orphanet:145 (MONDO:equivalentTo)
- SCTID:718220008 (MONDO:equivalentTo)
- GARD:0012351 (MONDO:equivalentTo)
- MESH:D061325 (MONDO:equivalentTo)
- NCIT:C8493 (MONDO:exact-label-match)
ordo_disease, predisposition, clingen
https://github.com/monarch-initiative/mondo/issues/84
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.
https://omim.org/phenotypicSeries/PS604370, http://purl.obolibrary.org/obo/Orphanet_145, http://identifiers.org/mesh/D061325, http://purl.obolibrary.org/obo/DOID_5683, http://purl.obolibrary.org/obo/NCIT_C8493, http://identifiers.org/snomedct/718220008, http://linkedlifedata.com/resource/umls/id/C0677776
http://purl.obolibrary.org/obo/MONDO_0016419, http://purl.obolibrary.org/obo/MONDO_0016248, http://purl.obolibrary.org/obo/MONDO_0015870
familial breast and ovarian cancer syndrome, hereditary breast and ovarian cancer syndrome, hereditary breast ovarian cancer syndrome, hereditary breast and ovarian cancer, BRCA1- and BRCA2-associated hereditary breast and ovarian cancer, BRCA1- and BRCA2-associated hereditary breast and ovarian cancer (HBOC), breast-ovarian cancer, familial, susceptibility to, hereditary breast/ovarian cancer (BRCA1, BRCA2), familial breast/ovarian cancer (BRCA1, BRCA2)
hereditary breast ovarian cancer, syndromes, HBOC, HBOC syndrome, syndrome, HBOC, HBOC syndromes
MONDO:0003582