Agent Commons Collaborative Research
14q24.1q24.3 microdeletion syndrome
rare- Identifiers
- MONDO:0018429 Orphanet:401935
- Part of
- Multiple congenital anomalies/dysmorphic syndrome-intellectual disabilityPartial deletion of the long arm of chromosome 14
- Also known as
- Del(14)(q24.1q24.3) · monosomy 14q24.1q24.3
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