About   Help   FAQ
Disease Ontology Browser
McCune Albright syndrome (DOID:1858)
Alliance: disease page
Synonyms: fibrous dysplasia of bone; osteitis fibrosa disseminata; polyostotic fibrous dysplasia
Alt IDs: OMIM:174800, DOID:11345, ICD10CM:Q78.1, ICD9CM:756.54, MESH:D005359, NCI:C34610, UMLS_CUI:C0016065
Definition: A syndrome that is characterized by polyostotic fibrous dysplasia, precocious puberty, and caf -au-lait spots and has_material_basis_in spontaneous post zygotic missense mutation at ARG201 or Gln227 of the GNAS gene during embryogenesis.

Disease References using Mouse Models (2)

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB), Gene Ontology (GO)
Citing These Resources
Funding Information
Warranty Disclaimer & Copyright Notice
Send questions and comments to User Support.
last database update
08/03/2022
MGI 6.21
The Jackson Laboratory