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Chromosome 15q13.3 microdeletion syndrome
rare15q13.3 microdeletion (microdel15q13.3) syndrome is characterized by a wide spectrum of neurodevelopmental disorders with no or subtle dysmorphic features.
- Identifiers
- MONDO:0012774 OMIM:612001Orphanet:199318
- Part of
- Congenital nervous system disorderMultiple congenital anomalies/dysmorphic syndrome-intellectual disabilityPartial deletion of the long arm of chromosome 15
- Also known as
- 15q13.3 microdeletion · 15q13.3 microdeletion syndrome · Del(15)(q13.3) · microdeletion 15q13.3 syndrome · monosomy 15q13.3
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