Human genes for McCune Albright syndrome
McCune Albright syndrome [DOID:1858]
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: McCune Albright syndrome, DOID:1858, McCune Albright disease, McCune Albright disorder, McCune Albright syndromes ...
Linkouts: OMIM