OBO ID: DOID:1858 |
Term Name: | McCune Albright syndrome | Search Ontology: | |
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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. (3) | ||
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Ontology: | Human Disease ( DOID:1858 ) |
OTHER McCune Albright syndrome PAGES
ZEBRAFISH MODELS
No data available
PHENOTYPE
No data available
CITATIONS: None
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