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Intellectual disability, autosomal recessive 5

MONDO:0012613

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

Also known as: NSUN2 autosomal recessive non-syndromic intellectual disability, autosomal recessive non-syndromic intellectual disability caused by mutation in NSUN2, intellectual disability, autosomal recessive 5, intellectual disability, autosomal recessive type 5, mental retardation, autosomal recessive type 5, MRT5, mental retardation, autosomal recessive 5

0 clinical trials for this condition and its sub-types, 0 tagged with Intellectual disability, autosomal recessive 5 itself.

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