|Dataset||OMIM 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 associated with the velocardiofacial syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.