Intellectual disability, autosomal recessive 2

MONDO:0011828

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

Also known as: CRBN autosomal recessive non-syndromic intellectual disability, autosomal recessive non-syndromic intellectual disability caused by mutation in CRBN, intellectual disability, autosomal recessive 2, intellectual disability, autosomal recessive type 2, mental retardation, autosomal recessive type 2, MRT2, intellectual disability, autosomal recessive 2A, mental retardation, autosomal recessive 2

0 clinical trials for this condition and its sub-types, 0 tagged with Intellectual disability, autosomal recessive 2 itself.

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↑ Autosomal recessive non-syndromic intellectual disability (0)

Including sub-types (0) Tagged with Intellectual disability, autosomal recessive 2 (0)

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