| Dataset | CTD Gene-Disease Associations |
| Category | disease or phenotype associations |
| Type | disease |
| Description | A chromosomal disease that has_material_basis_in deletion polymorphisms at chromosome location 22q11 and is characterized by variable developmental problems and schizoid features. (Human Disease Ontology, DOID_12583) |
| External Link | http://ctdbase.org/detail.go?type=disease&acc=MESH:D058165 |
| Similar Terms | |
| Downloads & Tools |
1 genes/proteins associated with the disease 22q11 Deletion Syndrome from the curated CTD Gene-Disease Associations dataset.
| Symbol | Name | Standardized Value |
|---|---|---|
| FGF8 | fibroblast growth factor 8 (androgen-induced) | 2.88009 |
