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Autosomal dominant syndromic intellectual disability

MONDO:0100601

Autosomal dominant form of syndromic intellectual disability.

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

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Sub-types

Severe intellectual disability-progressive spastic diplegia syndrome (4) Intellectual disability-severe speech delay-mild dysmorphism syndrome (2) KBG syndrome (2) Mowat-Wilson syndrome (2) Autism spectrum disorder due to AUTS2 deficiency (1) Bohring-Opitz syndrome (1) Chromosome 2q32-q33 deletion syndrome (1) Intellectual disability-microcephaly-strabismus-behavioral abnormalities syndrome (1) Schuurs-Hoeijmakers syndrome (1) ADNP-related multiple congenital anomalies - intellectual disability - autism spectrum disorder (0) Autosomal dominant intellectual disability-craniofacial anomalies-cardiac defects syndrome (0) Bosch-Boonstra-Schaaf optic atrophy syndrome (0) Cardiac anomalies - developmental delay - facial dysmorphism syndrome (0) CTCF-related neurodevelopmental disorder (0) DYRK1A-related intellectual disability syndrome (0) DYRK1A-related intellectual disability syndrome due to 21q22.13q22.2 microdeletion (0) Hereditary cryohydrocytosis with reduced stomatin (0) Houge-Janssens syndrome 1 (0) Intellectual developmental disorder with dysmorphic facies and behavioral abnormalities (0) Intellectual developmental disorder with dysmorphic facies and ptosis (0)

Broader categories

Disease (717) Nervous system disorder (243) Hereditary disease (188) Neurodevelopmental disorder (154) Intellectual disability (133) Syndromic disease (25) Human disease (15) Hereditary neurological disease (6) Disease of genetic or genomic mechanism (2) Syndromic intellectual disability (2)

Trials to join now! 9 Not yet recruiting 2 Not yet finished but already full! 3 Completed 1