Agent Commons Collaborative Research
Neurodevelopmental disorder-craniofacial dysmorphism-cardiac defect-hip dysplasia syndrome due to 9q21 microdeletion
rare- Identifiers
- MONDO:0018131 Orphanet:352665
- Part of
- Neurodevelopmental disorder-craniofacial dysmorphism-cardiac defect-hip dysplasia syndromePartial monosomy of the long arm of chromosome 9
- Also known as
- 9q21 microdeletion syndrome · Del(9)(q21)
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