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Intellectual disability, autosomal dominant 5

MONDO:0012960

Any autosomal dominant non-syndromic intellectual disability in which the cause of the disease is a mutation in the SYNGAP1 gene.

Also known as: MRD5, SYNGAP1 autosomal dominant non-syndromic intellectual disability, SYNGAP1-related developmental and epileptic encephalopathy, autosomal dominant intellectual disability 5, autosomal dominant non-syndromic intellectual disability caused by mutation in SYNGAP1, epilepsy due to SYNGAP mutations, intellectual disability, autosomal dominant 5, intellectual disability, autosomal dominant type 5

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

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Broader categories

Disease (618) Epilepsy (398) Nervous system disorder (217) Hereditary disease (172) Neurodevelopmental disorder (125) Intellectual disability (115) Brain disorder (110) Central nervous system disorder (97) Human disease (14) Hereditary neurological disease (5)

Trials to join now! 17 Not yet recruiting 5 Not yet finished but already full! 6 Completed 8

Intellectual disability, autosomal dominant 5

Broader categories

Real-World study tracks Epidyolex's Long-Term impact on seizures

AI boosts brain scan accuracy in massive new trial

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New framework aims to prevent medication errors in vulnerable group

300 volunteers help create medical image bank for science