22q11 Deletion Syndrome Gene Set

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
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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