autosomal genetic disease McCune Albright syndrome GARD:6995 OMIM mapping confirmed by DO. [SN]. ICD10CM:Q78.1 UMLS_CUI:C0016065 OMIM:174800 NCI:C34610 DOID:1858 DOID:11345 ICD9CM:756.54 disease_ontology A syndrome that is characterized by polyostotic fibrous dysplasia, precocious puberty, and café-au-lait spots and has_material_basis_in spontaneous post zygotic missense mutation at ARG201 or Gln227 of the GNAS gene during embryogenesis. SNOMEDCT_US_2020_03_01:726029005 MESH:D005359 fibrous dysplasia of bone osteitis fibrosa disseminata polyostotic fibrous dysplasia syndrome