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Disease Ontology Browser
velocardiofacial syndrome (DOID:12583)
Alliance: disease page
Synonyms: 22q11 Deletion Syndrome; deletion 22q11.2 syndrome; Shprintzen syndrome; VCF-Velocardiofacial syndrome
Alt IDs: OMIM:192430, ICD10CM:Q93.81, ICD9CM:758.32, MESH:D004062, UMLS_CUI:C0220704
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.

Disease References using Mouse Models (9)

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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last database update
11/28/2017
MGI 6.11
The Jackson Laboratory