Intellectual disability, autosomal dominant 33

MONDO:0014580

Any autosomal dominant non-syndromic intellectual disability in which the cause of the disease is a mutation in the DPP6 gene.

Also known as: DPP6 autosomal dominant non-syndromic intellectual disability, MRD33, autosomal dominant intellectual disability 33, autosomal dominant non-syndromic intellectual disability caused by mutation in DPP6, intellectual disability, autosomal dominant 33, intellectual disability, autosomal dominant type 33, mental retardation, autosomal dominant type 33, autosomal dominant non-syndromic intellectual disability 33

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 33

Broader categories

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