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Intellectual disability, autosomal dominant 13

MONDO:0013805

Any autosomal dominant non-syndromic intellectual disability in which the cause of the disease is a mutation in the DYNC1H1 gene.

Also known as: DYNC1H1 autosomal dominant non-syndromic intellectual disability, MRD13, autosomal dominant intellectual disability 13, autosomal dominant non-syndromic intellectual disability caused by mutation in DYNC1H1, intellectual disability, autosomal dominant 13, intellectual disability, autosomal dominant 13, with neuronal migration defects, intellectual disability, autosomal dominant type 13, mental retardation, autosomal dominant type 13

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

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Broader categories

Cardiovascular disorder (969) Disease (618) Nervous system disorder (217) Hereditary disease (172) Neurodevelopmental disorder (125) Vascular disorder (122) Intellectual disability (115) Eye disorder (97) Retinal disorder (79) Syndromic disease (24)
Trials to join now! 90 Not yet recruiting 34 Not yet finished but already full! 24 Completed 48 Terminated 4
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