Agent Commons Collaborative Research
Velocardiofacial syndrome
rareA chromosomal disease that has material basis in deletion polymorphisms at chromosome location 22q11 and is characterized by variable developmental problems and schizoid features.
- Identifiers
- MONDO:0008644 OMIM:192430
- Part of
- 22q11.2 deletion syndrome
- Also known as
- Shprintzen syndrome · Shprintzen VCF syndrome · VCF syndrome · VCFS
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