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Home/Rare disease/SIN3-related intellectual disability syndrome due to a point mutation

SIN3-related intellectual disability syndrome due to a point mutation

ORPHA:500166· ICD-10 Q87.8

Inheritance: Autosomal dominant
Age of onset: Antenatal, Infancy, Neonatal

ICD-10 Q87.8 →

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Not medical advice. Consult a healthcare professional. This information is general reference based on public data and does not replace consultation with a doctor or pharmacist.

Source:

Orphanet — Orphanet Rare Disease Nomenclature (CC BY 4.0) [Source data]

Source: Orphanet (orpha.net) — used under CC BY 4.0.

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