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

28 clinical trials for this condition and its sub-types.

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Broader categories

Disease (618) Nervous system disorder (217) Hereditary disease (172) Neurodevelopmental disorder (125) Intellectual disability (115) Human disease (14) Hereditary neurological disease (5) Disease of genetic or genomic mechanism (2) Autosomal dominant disease (0) Autosomal dominant non-syndromic intellectual disability (0)

Trials to join now! 12 Not yet recruiting 5 Not yet finished but already full! 3 Completed 8

Intellectual disability, autosomal dominant 22

Broader categories

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