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DYRK1A-related intellectual disability syndrome

MONDO:0013578

An autosomal dominant non-syndromic intellectual disability that has material basis in an autosomal dominant mutation of DYRK1A on chromosome 21q22.13.

Also known as: MRD7, autosomal dominant intellectual disability 7, intellectual disability, autosomal dominant type 7, mental retardation, autosomal dominant type 7, autosomal dominant non-syndromic intellectual disability 7, intellectual disability, autosomal dominant 7, mental retardation, autosomal dominant 7

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

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Sub-types

DYRK1A-related intellectual disability syndrome due to 21q22.13q22.2 microdeletion (0) Intellectual disability syndrome due to a DYRK1A point mutation (0)

Broader categories

Disease (618) Nervous system disorder (217) Hereditary disease (172) Neurodevelopmental disorder (125) Intellectual disability (115) Syndromic disease (24) Human disease (14) Developmental defect during embryogenesis (7) Hereditary neurological disease (5) Disease of genetic or genomic mechanism (2)
Trials to join now! 14 Not yet recruiting 5 Not yet finished but already full! 3 Completed 10
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