|Dataset||CTD Gene-Disease Associations|
|Category||disease or phenotype associations|
|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)|
|Downloads & Tools|
1 genes/proteins associated with the disease 22q11 Deletion Syndrome from the curated CTD Gene-Disease Associations dataset.
|FGF8||fibroblast growth factor 8 (androgen-induced)||2.88009|