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

Disease Ontology Definition:An autosomal dominant disease that involves skin pigmentation, bone and hormonal problems along with premature puberty. It has material basis in mutations in the GNAS1 gene.

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

Echinobase Genes :


OMIM:
MIM:174800 - mccune-albright syndrome; mas

Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s): autosomal dominant disease (is_a)