Intellectual disability, autosomal recessive 34

rare

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

Identifiers: MONDO:0013785 OMIM:614499
Causal genes: CRADD
Part of: Autosomal recessive non-syndromic intellectual disability
Also known as: autosomal recessive non-syndromic intellectual disability caused by mutation in CRADD · CRADD autosomal recessive non-syndromic intellectual disability · intellectual developmental disorder, autosomal recessive 34, with variant lissencephaly · intellectual disability, autosomal recessive type 34 · mental retardation, autosomal recessive 34

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