greig cephalopolysyndactyly syndrome Gene Set

Dataset OMIM Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
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)
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1 genes associated with the greig cephalopolysyndactyly syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.

Symbol Name
GLI3 GLI family zinc finger 3