Orphanet: SIN3A related intellectual disability syndrome due to a point mutation

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ORPHA:500166

Classification level: Subtype of disorder

Synonym(s): -
Prevalence: -
Inheritance: Autosomal dominant
Age of onset: Antenatal, Neonatal, Infancy
ICD-10: Q87.8
OMIM: 613406
UMLS: C5681223
MeSH: -
GARD: -
MedDRA: -

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SIN3A-related intellectual disability syndrome due to a point mutation

ORPHA:500166

Summary

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