Shprintzen syndrome Gene Set

Dataset ClinVar Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
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)
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1 genes associated with the Shprintzen syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Symbol Name
TBX1 T-box 1