|Dataset||HuGE Navigator Gene-Phenotype 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|
3 genes associated with the 22q11 Deletion Syndrome phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.