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Autosomal dominant non-syndromic intellectual disability

MONDO:0015802

Autosomal dominant form of non-syndromic intellectual disability.

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

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

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Sub-types

Intellectual developmental disorder 61 (5) Intellectual developmental disorder 62 (1) Intellectual disability, autosomal dominant 43 (1) Neurodevelopmental disorder with hypotonia, stereotypic hand movements, and impaired language (1) Clark-Baraitser syndrome (0) Coffin-Siris syndrome 6 (0) Intellectual developmental disorder 59 (0) Intellectual developmental disorder 60 with seizures (0) Intellectual developmental disorder, autosomal dominant 63, with macrocephaly (0) Intellectual developmental disorder, autosomal dominant 73 (0) Intellectual disability, autosomal dominant 22 (0) Intellectual disability, autosomal dominant 33 (0) Intellectual disability, autosomal dominant 34 (0) Intellectual disability, autosomal dominant 41 (0) Intellectual disability, autosomal dominant 45 (0) Intellectual disability, autosomal dominant 46 (0) Intellectual disability, autosomal dominant 47 (0) Intellectual disability, autosomal dominant 50 (0) Intellectual disability, autosomal dominant 51 (0) Intellectual disability, autosomal dominant 52 (0)

Broader categories

Disease (680) Nervous system disorder (231) Hereditary disease (176) Neurodevelopmental disorder (147) Intellectual disability (133) Human disease (14) Hereditary neurological disease (6) Disease of genetic or genomic mechanism (2) Autosomal dominant disease (0) Autosomal genetic disease (0)

Trials to join now! 5 Not yet recruiting 2 Completed 1