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Intellectual disability, autosomal dominant 43

MONDO:0014858

Any autosomal dominant non-syndromic intellectual disability in which the cause of the disease is a mutation in the HIVEP2 gene.

Also known as: HIVEP2 autosomal dominant non-syndromic intellectual disability, MRD43, autosomal dominant intellectual disability 43, autosomal dominant non-syndromic intellectual disability caused by mutation in HIVEP2, intellectual disability, autosomal dominant 43, intellectual disability, autosomal dominant type 43, mental retardation, autosomal dominant 43, mental retardation, autosomal dominant type 43

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
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