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Neurodevelopmental disorder-craniofacial dysmorphism-cardiac defect-skeletal anomalies syndrome due to 9q21.3 microdeletion
ORPHA:352665
Classification level: Subtype of disorder- Synonym(s):
- 9q21.3 microdeletion syndrome
- Del(9)(q21.3)
- Prevalence: <1 / 1 000 000
- Inheritance: Not applicable or Unknown
- Age of onset: Infancy, Neonatal
- ICD-10: Q93.5
- OMIM: 616580
- UMLS: C5679925
- MeSH: -
- GARD: -
- MedDRA: -
Summary
This disease is described under Neurodevelopmental disorder-craniofacial dysmorphism-cardiac defect-skeletal anomalies syndrome
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