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Home/Rare disease/Brain abnormalities-severe developmental delay-facial dysmorphism-intellectual disability syndrome due to MEF2C mutation

Brain abnormalities-severe developmental delay-facial dysmorphism-intellectual disability syndrome due to MEF2C mutation

ORPHA:664416

Inheritance: Autosomal dominant

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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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