Click here to close Hello! We notice that you are using Internet Explorer, which is not supported by Xenbase and may cause the site to display incorrectly. We suggest using a current version of Chrome, FireFox, or Safari.
Summary Literature (0)
DOID:1858 - McCune Albright syndrome


Disease Ontology Definition: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.

Synonyms: fibrous Dysplasia of bone, fibrous dysplasia of bone, fibrous dysplasia of bone (disorder), osteitis fibrosa disseminata, polyostotic fibrous dysplasia

In OMIM:
OMIM:174800 - MCCUNE-ALBRIGHT SYNDROME; MAS

In Mondo Disease Ontology:
MONDO:0018919 - McCune-Albright syndrome

Human Disease Resources: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee

Xenbase Genes : gnas

Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD
Parent(s): autosomal dominant disease (is_a), autosomal genetic disease (is_a), syndrome (is_a)