syndrome caused by partial chromosomal deletion velocardiofacial syndrome 22q11 deletion syndrome A chromosomal disease that has material basis in deletion polymorphisms at chromosome location 22q11 and is characterized by variable developmental problems and schizoid features. DOID:12583 ICD10:Q93.81 ICD9:758.32 MONDO:0008644 OMIM:192430 Shprintzen Vcf syndrome Shprintzen syndrome UMLS:CN205308 VCF-velocardiofacial syndrome Vcf syndrome chromosome 22Q11.2 deletion syndrome deletion 22q11.2 syndrome velocardiofacial syndrome 22q11.2 deletion syndrome