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McCune-Albright syndrome

Go to external page http://purl.obolibrary.org/obo/MONDO_0018919

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). [ Orphanet:562 ]

Synonyms: Albright's disease McCune Albright Syndrome mccune-albright syndrome, somatic, mosaic gonadotropin-independent female-limited sexual precocity MAS McCune Albright syndrome

This is just here as a test because I lose it

Term information

database cross reference
  • NANDO:2200412 (https://orcid.org/0000-0003-0011-764X)
  • icd11.foundation:132749439 (MONDO:equivalentTo)
  • ICD10CM:Q78.1 (Orphanet:562/ntbt)
  • NCIT:C48627 (https://orcid.org/0000-0002-6601-2165)
  • MESH:D005359 (Orphanet:562/e)
  • SCTID:726029005 (MONDO:equivalentTo)
  • UMLS:C0242292 (MONDO:equivalentTo)
  • Orphanet:562 (MONDO:equivalentTo)
  • OMIM:174800 (Orphanet:562/e)
  • DOID:1858 (MONDO:equivalentTo)
  • NORD:1413 (MONDO:NORD)
  • GARD:6995 (MONDO:GARD)
  • MEDGEN:69164 (MONDO:equivalentTo)
Subsets

gard_rare, ordo_disorder, matrix_llm__is_cancer_other, matrix_llm__is_glucose_dysfunction_other, otar, matrix_llm__tag_qualy_lost_other, mondo_top_grouping_member, matrix_llm__txgnn_other, matrix_llm__medical_specialization_other, mondo_top_grouping_hereditary_disease, mondo_top_grouping_musculoskeletal_system_disorder, matrix_llm__tag_existing_treatment_other, matrix_included, nord_rare, matrix_txgnn_grouping_other, matrix_llm__anatomical_other, matrix_llm__is_pathogen_caused_other, rare, harrisons_view_member, harrisons_view_syndromic_disease, harrisons_view_musculoskeletal_system_disorder, harrisons_view_hereditary_disease, orphanet_rare, mondo_top_grouping_syndromic_disease

abbreviation
POFD [ GARD:0006995 ]

abbreviation
PFD [ GARD:0006995 ]

exactMatch

https://omim.org/entry/174800

http://purl.obolibrary.org/obo/mondo/sources/icd11foundation/132749439

http://purl.obolibrary.org/obo/NCIT_C48627

http://identifiers.org/medgen/69164

http://identifiers.org/snomedct/726029005

http://linkedlifedata.com/resource/umls/id/C0242292

http://www.orpha.net/ORDO/Orphanet_562

http://purl.obolibrary.org/obo/DOID_1858

excluded subClassOf

http://purl.obolibrary.org/obo/MONDO_0019708

http://purl.obolibrary.org/obo/MONDO_0015945

http://purl.obolibrary.org/obo/MONDO_0000426

has related synonym

polyostotic fibrous dysplasia

POFD

PFD

id

MONDO:0018919

term tracker item

https://github.com/monarch-initiative/mondo/issues/6751

https://github.com/monarch-initiative/mondo/issues/4521

https://github.com/monarch-initiative/mondo/issues/4948