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Echinobase
Summary Literature (0)
DOID:12583 - velocardiofacial syndrome

Disease Ontology Definition:A chromosomal disease that has_material_basis_in deletion polymorphisms at chromosome location 22q11 and is characterized by variable developmental problems and schizoid features.

Synonyms: 22q11 Deletion Syndrome, Shprintzen syndrome, VCF-Velocardiofacial syndrome, deletion 22q11.2 syndrome,

Echinobase Genes : tbx1


OMIM:
MIM:192430 - velocardiofacial syndrome

Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s): chromosomal deletion syndrome (is_a)