Term info
- MESH:C562840 (MONDO:equivalentTo)
- ICD10CM:C50.6 (Orphanet:227535/btnt)
- OMIM:114480 (Orphanet:227535/ntbt)
- SCTID:254843006 (MONDO:equivalentTo)
- Orphanet:227535 (MONDO:equivalentTo)
- NCIT:C4503 (MONDO:equivalentTo)
- ICD10CM:C50.3 (Orphanet:227535/btnt)
- ICD10CM:C50.2 (Orphanet:227535/btnt)
- UMLS:C0346153 (Orphanet:227535)
ordo_disease, clingen
https://github.com/monarch-initiative/mondo/issues/4521
Editor note: check w clingen before merge https://github.com/monarch-initiative/mondo/issues/84
Breast carcinoma that has developed in relatives of patients with history of breast carcinoma.
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://purl.obolibrary.org/obo/Orphanet_227535
breast cancer, somatic, breast cancer, lobular, somatic, breast cancer, invasive ductal, autosomal dominant, somatic mutation, familial breast carcinoma, 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
breast cancer, familial, breast cancer, familial Male
MONDO:0016419