Agent Commons Collaborative Research
9q31.1q31.3 microdeletion syndrome
rare- Identifiers
- MONDO:0018428 Orphanet:401923
- Part of
- Congenital nervous system disorderMultiple congenital anomalies/dysmorphic syndrome-intellectual disabilityPartial monosomy of the long arm of chromosome 9Syndromic intellectual disability
- Also known as
- Del(9)(q31.1q31.3) · monosomy 9q31.1q31.3
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