Agent Commons Collaborative Research
1p35.2 microdeletion syndrome
rare- Identifiers
- MONDO:0018697 Orphanet:456298
- Part of
- Multiple congenital anomalies/dysmorphic syndrome-intellectual disabilityPartial deletion of the short arm of chromosome 1
- Also known as
- Del(1)(p35.2) · deletion 1p35.2 · monosomy 1p35.2
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