Breast carcinoma that has developed in relatives of patients with history of breast carcinoma. [ NCIT:P378 ]
Synonyms: breast cancer, somatic breast cancer, lobular, somatic familial breast carcinoma breast cancer, invasive ductal, autosomal dominant, somatic mutation breast cancer, susceptibility to, autosomal dominant, somatic mutation breast cancer, male, susceptibility to, autosomal dominant, somatic mutation breast cancer, protection against, autosomal dominant, somatic mutation hereditary breast carcinoma hereditary breast cancer breast cancer susceptibility, autosomal dominant, somatic mutation familial breast cancer breast cancer, early-onset, susceptibility to, autosomal dominant, somatic mutation familial cancer of the breast familial cancer of breast
Term information
- MESH:C562840 (MONDO:equivalentTo)
- ICD10CM:C50.3 (Orphanet:227535/btnt)
- ICD10CM:C50.2 (Orphanet:227535/btnt)
- UMLS:C0346153 (MONDO:equivalentTo)
- GARD:17142 (MONDO:GARD)
- SCTID:254843006 (MONDO:equivalentTo)
- MEDGEN:87542 (MONDO:equivalentTo)
- Orphanet:227535 (MONDO:equivalentTo)
- ICD10CM:C50.6 (Orphanet:227535/btnt)
- NCIT:C4503 (MONDO:equivalentTo)
- OMIM:114480 (Orphanet:227535/ntbt)
gard_rare, ordo_disorder, otar, rare, nord_rare, orphanet_rare, clingen
Editor note: check w clingen before merge https://github.com/monarch-initiative/mondo/issues/84
http://identifiers.org/snomedct/254843006
http://linkedlifedata.com/resource/umls/id/C0346153
http://purl.obolibrary.org/obo/NCIT_C4503
http://identifiers.org/mesh/C562840
https://omim.org/entry/114480
http://www.orpha.net/ORDO/Orphanet_227535
http://identifiers.org/medgen/87542