|Dataset||OMIM Gene-Disease Associations|
|Category||disease or phenotype associations|
|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)|
|Downloads & Tools|
1 genes associated with the greig cephalopolysyndactyly syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.
|GLI3||GLI family zinc finger 3|