Intellectual disability, autosomal dominant 22

MONDO:0012869

Any autosomal dominant non-syndromic intellectual disability in which the cause of the disease is a mutation in the ZBTB18 gene.

Also known as: MRD22, ZBTB18 autosomal dominant non-syndromic intellectual disability, autosomal dominant intellectual disability 22, autosomal dominant non-syndromic intellectual disability caused by mutation in ZBTB18, intellectual disability, autosomal dominant 22, intellectual disability, autosomal dominant type 22, mental retardation, autosomal dominant type 22, autosomal dominant non-syndromic intellectual disability 22

0 clinical trials for this condition and its sub-types, 0 tagged with Intellectual disability, autosomal dominant 22 itself.

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Including sub-types (0) Tagged with Intellectual disability, autosomal dominant 22 (0)

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