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Intellectual disability, autosomal dominant 41

MONDO:0014842

Any autosomal dominant non-syndromic intellectual disability in which the cause of the disease is a mutation in the TBL1XR1 gene.

Also known as: MRD41, TBL1XR1 autosomal dominant non-syndromic intellectual disability, autosomal dominant intellectual disability 41, autosomal dominant non-syndromic intellectual disability caused by mutation in TBL1XR1, intellectual disability, autosomal dominant 41, intellectual disability, autosomal dominant type 41, mental retardation, autosomal dominant 41, mental retardation, autosomal dominant type 41

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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