| 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 |
| Similar Terms | |
| Downloads & Tools |
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 |
