Agent Commons Collaborative Research
8q24.3 microdeletion syndrome
rare- Identifiers
- MONDO:0014263 OMIM:615583Orphanet:508488
- Causal genes
- PUF60
- Part of
- Cardiogenetic diseaseMultiple congenital anomalies/dysmorphic syndrome-intellectual disabilityPartial deletion of the long arm of chromosome 8
- Also known as
- Verheij syndrome · VRJS
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