intellectual disability, autosomal dominant 2

Rare Disease

MONDO:0013581

Also known as:

DOCK8 autosomal dominant non-syndromic intellectual disabilityMRD2autosomal dominant intellectual disability 2

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

Genes

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Clinical Trials

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Newborn Screening

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Patient Groups

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intellectual disability, autosomal dominant 2

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