Intellectual disability, autosomal recessive 3

rare

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

Identifiers: MONDO:0012037 OMIM:608443
Causal genes: CC2D1A
Part of: Autosomal recessive non-syndromic intellectual disability
Also known as: autosomal recessive non-syndromic intellectual disability caused by mutation in CC2D1A · CC2D1A autosomal recessive non-syndromic intellectual disability · intellectual disability, autosomal recessive type 3 · mental retardation, autosomal recessive 3 · mental retardation, autosomal recessive type 3

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