Intellectual disability, autosomal recessive 3

MONDO:0012037

Any autosomal recessive non-syndromic intellectual disability in which the cause of the disease is a mutation in the CC2D1A gene.

Also known as: CC2D1A autosomal recessive non-syndromic intellectual disability, MRT3, autosomal recessive non-syndromic intellectual disability caused by mutation in CC2D1A, intellectual disability, autosomal recessive 3, intellectual disability, autosomal recessive type 3, mental retardation, autosomal recessive 3, mental retardation, autosomal recessive type 3

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↑ Autosomal recessive non-syndromic intellectual disability (0)

Including sub-types (0) Tagged with Intellectual disability, autosomal recessive 3 (0)

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