velocardiofacial syndrome

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Disease Overview

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 VCF syndrome
  • Shprintzen syndrome
  • VCF syndrome
  • VCF-velocardiofacial syndrome
  • chromosome 22Q11.2 deletion syndrome
  • deletion 22q11.2 syndrome
  • velocardiofacial syndrome22q11 deletion syndrome
  • Shprintzen VCF syndrome
  • Shprintzen syndrome
  • VCF syndrome
  • VCF-velocardiofacial syndrome
  • chromosome 22Q11.2 deletion syndrome
  • deletion 22q11.2 syndrome
  • velocardiofacial syndrome