Intellectual disability, autosomal recessive 47

MONDO:0014524

Any autosomal recessive non-syndromic intellectual disability in which the cause of the disease is a mutation in the FMN2 gene.

Also known as: FMN2 autosomal recessive non-syndromic intellectual disability, autosomal recessive non-syndromic intellectual disability caused by mutation in FMN2, intellectual developmental disorder, autosomal recessive 47, intellectual disability, autosomal recessive 47, intellectual disability, autosomal recessive type 47, mental retardation, autosomal recessive type 47, MRT47, mental retardation, autosomal recessive 47

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↑ Autosomal recessive non-syndromic intellectual disability (0)

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