Fibrous Dysplasia of Bone Gene Set

Dataset CTD Gene-Disease Associations
Category disease or phenotype associations
Type disease
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://ctdbase.org/detail.go?type=disease&acc=MESH:D005357
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Genes

2 genes/proteins associated with the disease Fibrous Dysplasia of Bone from the curated CTD Gene-Disease Associations dataset.

Symbol Name Standardized Value
FOS FBJ murine osteosarcoma viral oncogene homolog 2.88009
TRIM37 tripartite motif containing 37 2.88009