polyostotic fibrous dysplasia Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description An autosomal dominant disease that involves skin pigmentation, bone and hormonal problems along with premature puberty. It is caused by mutations in the GNAS1 gene. (Human Disease Ontology, DOID_1858)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0010735
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Genes

1 genes associated with the polyostotic fibrous dysplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
GNAS GNAS complex locus