Intellectual disability, autosomal dominant
MONDO:0100172Also known as: mental retardation, autosomal dominant, autosomal dominant intellectual disability
23 clinical trials for this condition and its sub-types, 0 tagged with Intellectual disability, autosomal dominant itself.
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Sub-types of Intellectual disability, autosomal dominant
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Autosomal dominant syndromic intellectual disability 0 trials · 15 incl. sub-types
34 sub-types
- Severe intellectual disability-progressive spastic diplegia syndrome 4 trials
- KBG syndrome 2 trials
- Mowat-Wilson syndrome 2 trials Sub-types →
- Intellectual disability-severe speech delay-mild dysmorphism syndrome 2 trials
- Bohring-Opitz syndrome 1 trial
- SATB2 associated disorder 0 trials · 1 incl. sub-types Sub-types →
- Schuurs-Hoeijmakers syndrome 1 trial
- Autism spectrum disorder due to AUTS2 deficiency 1 trial
- Intellectual disability-microcephaly-strabismus-behavioral abnormalities syndrome 1 trial
- ADNP-related multiple congenital anomalies - intellectual disability - autism spectrum disorder 0 trials
- Bosch-Boonstra-Schaaf optic atrophy syndrome 0 trials
- CTCF-related neurodevelopmental disorder 0 trials
- DYRK1A-related intellectual disability syndrome 0 trials Sub-types →
- Houge-Janssens syndrome 1 0 trials
- Myhre syndrome 0 trials
- Pierpont syndrome 0 trials
- Rubinstein-Taybi syndrome due to CREBBP mutations 0 trials
- Rubinstein-Taybi syndrome due to EP300 haploinsufficiency 0 trials
- SETD2-related microcephaly-severe intellectual disability-multiple congenital anomalies syndrome 0 trials
- SIN3A-related intellectual disability syndrome 0 trials Sub-types →
- Schinzel-Giedion syndrome 0 trials
- Ververi-Brady syndrome 1 0 trials
- Autosomal dominant intellectual disability-craniofacial anomalies-cardiac defects syndrome 0 trials
- Cardiac anomalies - developmental delay - facial dysmorphism syndrome 0 trials
- Hereditary cryohydrocytosis with reduced stomatin 0 trials
- Intellectual developmental disorder with dysmorphic facies and behavioral abnormalities 0 trials
- Intellectual developmental disorder with dysmorphic facies and ptosis 0 trials
- Intellectual developmental disorder with gastrointestinal difficulties and high pain threshold 0 trials
- Intellectual developmental disorder with speech delay, dysmorphic facies, and t-cell abnormalities 0 trials
- Intellectual disability, autosomal dominant 13 0 trials
- Intellectual disability, autosomal dominant 48 0 trials
- Intellectual disability-sparse hair-brachydactyly syndrome 0 trials
- Micrognathia-recurrent infections-behavioral abnormalities-mild intellectual disability syndrome 0 trials
- Severe intellectual disability-poor language-strabismus-grimacing face-long fingers syndrome 0 trials
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Autosomal dominant non-syndromic intellectual disability 0 trials · 8 incl. sub-types
26 sub-types
- Intellectual developmental disorder 61 5 trials
- Intellectual developmental disorder 62 1 trial
- Intellectual disability, autosomal dominant 43 1 trial
- Neurodevelopmental disorder with hypotonia, stereotypic hand movements, and impaired language 1 trial
- Clark-Baraitser syndrome 0 trials
- Coffin-Siris syndrome 6 0 trials
- Intellectual developmental disorder 59 0 trials
- Intellectual developmental disorder 60 with seizures 0 trials
- Intellectual developmental disorder, autosomal dominant 63, with macrocephaly 0 trials
- Intellectual developmental disorder, autosomal dominant 73 0 trials
- Intellectual disability, autosomal dominant 22 0 trials
- Intellectual disability, autosomal dominant 33 0 trials
- Intellectual disability, autosomal dominant 34 0 trials
- Intellectual disability, autosomal dominant 41 0 trials
- Intellectual disability, autosomal dominant 45 0 trials
- Intellectual disability, autosomal dominant 46 0 trials
- Intellectual disability, autosomal dominant 47 0 trials
- Intellectual disability, autosomal dominant 50 0 trials
- Intellectual disability, autosomal dominant 51 0 trials
- Intellectual disability, autosomal dominant 52 0 trials
- Intellectual disability, autosomal dominant 53 0 trials
- Intellectual disability, autosomal dominant 54 0 trials
- Intellectual disability, autosomal dominant 55, with seizures 0 trials
- Intellectual disability, autosomal dominant 56 0 trials
- Intellectual disability, autosomal dominant 57 0 trials
- Intellectual disability, autosomal dominant 58 0 trials
Most studied deeper sub-types
Chromosome 2q32-q33 deletion syndrome
(1)
DYRK1A-related intellectual disability syndrome due to 21q22.13q22.2 microdeletion
(0)
Intellectual disability syndrome due to a DYRK1A point mutation
(0)
Mowat-Wilson syndrome due to a ZEB2 point mutation
(0)
Mowat-Wilson syndrome due to monosomy 2q22
(0)
SIN3A-related intellectual disability syndrome due to a point mutation
(0)
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