Intellectual disability, autosomal recessive 59

MONDO:0015020

Any autosomal recessive non-syndromic intellectual disability in which the cause of the disease is a mutation in the IMPA1 gene.

Also known as: IMPA1 autosomal recessive non-syndromic intellectual disability, MRT59, autosomal recessive non-syndromic intellectual disability caused by mutation in IMPA1, intellectual disability, autosomal recessive 59, intellectual disability, autosomal recessive type 59, mental retardation, autosomal recessive 59, mental retardation, autosomal recessive type 59

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↑ Autosomal recessive non-syndromic intellectual disability (0)

Including sub-types (0) Tagged with Intellectual disability, autosomal recessive 59 (0)

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