| 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) |
| External Link | http://www.omim.org/entry/175700 |
| Similar Terms | |
| Downloads & Tools |
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 |
