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Neurodevelopmental disorder with or without hyperkinetic movements and seizures, autosomal dominant

MONDO:0013655

Any autosomal dominant non-syndromic intellectual disability in which the cause of the disease is a mutation in the GRIN1 gene.

Also known as: GRIN1 autosomal dominant non-syndromic intellectual disability, MRD8, NDHMSD, autosomal dominant intellectual disability 8, autosomal dominant non-syndromic intellectual disability caused by mutation in GRIN1, intellectual disability, autosomal dominant 8, intellectual disability, autosomal dominant type 8, mental retardation, autosomal dominant 8

29 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) Complex neurodevelopmental disorder (3) Disease of genetic or genomic mechanism (2) GRIN-related complex neurodevelopmental disorder (2)
Trials to join now! 12 Not yet recruiting 5 Not yet finished but already full! 3 Completed 9
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