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Intellectual disability, autosomal dominant 6

MONDO:0013509

Any autosomal dominant non-syndromic intellectual disability in which the cause of the disease is a mutation in the GRIN2B gene.

Also known as: GRIN2B encephalopathy, GRIN2B-related neurodevelopmental disorder, GRIN2B autosomal dominant non-syndromic intellectual disability, GRIN2B-related developmental delay, intellectual disability and autism spectrum disorder, MRD6, autosomal dominant non-syndromic intellectual disability caused by mutation in GRIN2B, intellectual developmental disorder, autosomal dominant 6, with or without seizures, intellectual disability, autosomal dominant 6

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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