intellectual disability, autosomal recessive 2

Rare Disease

MONDO:0011828

Also known as:

CRBN autosomal recessive non-syndromic intellectual disabilityautosomal recessive non-syndromic intellectual disability caused by mutation in CRBNintellectual disability, autosomal recessive 2

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

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