Term info
- DOID:1858 (MONDO:equivalentTo)
- ICD10CM:Q78.1 (Orphanet:562/ntbt)
- UMLS:C0242292 (Orphanet:562/e)
- OMIM:174800 (Orphanet:562/e)
- GARD:0006995 (MONDO:equivalentTo)
- SCTID:726029005 (MONDO:equivalentTo)
- NCIT:C48627 (MONDO:equivalentTo)
- UMLS:C0016065 (Orphanet:93276/e)
- Orphanet:562 (MONDO:equivalentTo)
- MESH:D005359 (Orphanet:562/e)
ordo_disease
https://github.com/monarch-initiative/mondo/issues/4521, https://github.com/monarch-initiative/mondo/issues/4948
McCune-Albright syndrome (MAS) is classically defined by the clinical triad of fibrous dysplasia of bone (FD), cafe-au-lait skin spots, and precocious puberty (PP).
https://omim.org/entry/174800, http://purl.obolibrary.org/obo/NCIT_C48627, http://purl.obolibrary.org/obo/Orphanet_562, http://linkedlifedata.com/resource/umls/id/C0016065, http://identifiers.org/snomedct/726029005, http://linkedlifedata.com/resource/umls/id/C0242292, http://purl.obolibrary.org/obo/DOID_1858
http://purl.obolibrary.org/obo/MONDO_0019708, http://purl.obolibrary.org/obo/MONDO_0015945, http://purl.obolibrary.org/obo/MONDO_0000426
Albright's disease, mccune-albright syndrome, somatic, mosaic, gonadotropin-independent female-limited sexual precocity, MAS, McCune Albright syndrome
polyostotic fibrous dysplasia, POFD, PFD
MONDO:0018919