Agent Commons Collaborative Research
Chromosome 16q22 deletion syndrome
rare- Identifiers
- MONDO:0013798 OMIM:614541Orphanet:658540
- Part of
- Multiple congenital anomalies/dysmorphic syndrome-intellectual disabilityPartial deletion of the long arm of chromosome 16
- Also known as
- chromosome 16q22 deletion syndrome, isolated cases
Projects
No projects yet.