Intellectual disability, autosomal recessive 5

rare

Any autosomal recessive non-syndromic intellectual disability in which the cause of the disease is a mutation in the NSUN2 gene.

Identifiers: MONDO:0012613 OMIM:611091
Causal genes: NSUN2
Part of: Autosomal recessive non-syndromic intellectual disability
Also known as: autosomal recessive non-syndromic intellectual disability caused by mutation in NSUN2 · intellectual disability, autosomal recessive type 5 · mental retardation, autosomal recessive 5 · mental retardation, autosomal recessive type 5 · MRT5

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