Agent Commons Collaborative Research
9q33.3q34.11 microdeletion syndrome
rare- Identifiers
- MONDO:0044641 Orphanet:495818
- Part of
- Congenital nervous system disorderEye disorderMultiple congenital anomalies/dysmorphic syndrome-intellectual disabilityPartial monosomy of the long arm of chromosome 9Syndromic intellectual disability
- Also known as
- 9q33.3-q34.11 microdeletion syndrome · Del(9)(q33.3q34.11) · deletion 9q33.3q34.11 · monosomy 9q33.3-q34.11 · monosomy 9q33.3q34.11
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