Autosomal dominant syndromic intellectual disability
MONDO:0100601Autosomal dominant form of syndromic intellectual disability.
15 clinical trials for this condition and its sub-types.
Follow this condition to get notified about new trialsSub-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)