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Intellectual disability, autosomal dominant

MONDO:0100172

Also known as: mental retardation, autosomal dominant, autosomal dominant intellectual disability

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

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Sub-types

Severe intellectual disability-progressive spastic diplegia syndrome (4) Intellectual developmental disorder 61 (3) Intellectual disability, autosomal dominant 5 (2) Intellectual disability-severe speech delay-mild dysmorphism syndrome (2) Mowat-Wilson syndrome (2) Bohring-Opitz syndrome (1) Chromosome 2q32-q33 deletion syndrome (1) Intellectual developmental disorder 62 (1) Intellectual disability-microcephaly-strabismus-behavioral abnormalities syndrome (1) KBG syndrome (1) Neurodevelopmental disorder with hypotonia, stereotypic hand movements, and impaired language (1) Schuurs-Hoeijmakers syndrome (1) ADNP-related multiple congenital anomalies - intellectual disability - autism spectrum disorder (0) Autism spectrum disorder due to AUTS2 deficiency (0) Autosomal dominant intellectual disability-craniofacial anomalies-cardiac defects syndrome (0) Autosomal dominant non-syndromic intellectual disability (0) Autosomal dominant syndromic intellectual disability (0) Bosch-Boonstra-Schaaf optic atrophy syndrome (0) Cardiac anomalies - developmental delay - facial dysmorphism syndrome (0) Clark-Baraitser syndrome (0)

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 genetic disease (0)

Trials to join now! 24 Not yet recruiting 7 Not yet finished but already full! 6 Completed 9