Intellectual disability, autosomal dominant 2

rare

Any autosomal dominant non-syndromic intellectual disability in which the cause of the disease is a mutation in the DOCK8 gene.

Identifiers: MONDO:0013581 OMIM:614113
Causal genes: DOCK8
Part of: Intellectual disability, autosomal dominant
Also known as: autosomal dominant intellectual disability 2 · autosomal dominant non-syndromic intellectual disability caused by mutation in DOCK8 · DOCK8 autosomal dominant non-syndromic intellectual disability · intellectual disability, autosomal dominant type 2 · mental retardation, autosomal dominant 2

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