Intellectual disability, autosomal recessive 2

rare

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

Identifiers: MONDO:0011828 OMIM:607417
Causal genes: CRBN
Part of: Autosomal recessive non-syndromic intellectual disability
Also known as: autosomal recessive non-syndromic intellectual disability caused by mutation in CRBN · CRBN autosomal recessive non-syndromic intellectual disability · intellectual disability, autosomal recessive type 2 · mental retardation, autosomal recessive 2 · mental retardation, autosomal recessive 2A

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