chromosomal deletion syndrome velocardiofacial syndrome SNOMEDCT_US_2020_03_01:205642004 disease_ontology UMLS_CUI:C0220704 A chromosomal deletion disease that has_material_basis_in deletion polymorphisms at chromosome location 22q11 and that is characterized by variable developmental problems and schizoid features. OMIM mapping confirmed by DO. [LS]. ICD10CM:Q93.81 22q11 Deletion Syndrome ICD9CM:758.32 MESH:D004062 DOID:12583 OMIM:192430 Shprintzen syndrome VCF-Velocardiofacial syndrome deletion 22q11.2 syndrome