Greig cephalopolysyndactyly syndrome Gene Set

Dataset CTD Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description An acrocephalosyndactylia that has_material_basis_in mutation in the GLI3 gene which results_in abnormal development located_in limb, located_in head, located_in face. (Human Disease Ontology, DOID_14761)
External Link http://ctdbase.org/detail.go?type=disease&acc=MESH:C537300
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Genes

1 genes/proteins associated with the disease Greig cephalopolysyndactyly syndrome from the curated CTD Gene-Disease Associations dataset.

Symbol Name Standardized Value
GLI3 GLI family zinc finger 3 2.88009