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
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One-Patient trial aims to treat Ultra-Rare genetic disorder
Disease control Not yet recruitingThis study tests a custom-made drug called an antisense oligonucleotide (ASO) designed for one person with Schuurs-Hoeijmakers syndrome, a rare genetic condition. The drug aims to correct a specific genetic mutation to improve communication and motor skills. Only one participant …
Phase 1/2 • Sponsor: n-Lorem Foundation • Aim: Disease control
Last updated Jun 27, 2026 11:01 UTC
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Saliva test may unlock genetic secrets missed by blood tests
Diagnosis Not yet recruitingThis study tests whether a simple saliva swab can find genetic causes of neurodevelopmental or intellectual disorders when standard blood tests have not. Researchers will use advanced DNA sequencing on cheek cells from 50 participants. The goal is to improve diagnosis and help gu…
Sponsor: Centre Hospitalier Universitaire de Besancon • Aim: Diagnosis
Last updated Jun 27, 2026 12:07 UTC
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Thinking through tasks: a new therapy aims to help kids with intellectual disability master daily life
Symptom relief Not yet recruitingThis pilot study tests a therapy protocol based on cognitive-occupational principles (CO-OP) for children and adolescents aged 10-21 with mild to moderate intellectual disability. The intervention involves weekly 45-minute sessions over 12-15 weeks, delivered by occupational ther…
Sponsor: Miri Tal-Saban • Aim: Symptom relief
Last updated Aug 13, 2026 00:00 UTC
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Rare syndrome study aims to map dental and facial patterns
Knowledge-focused Not yet recruitingThis study looks at the teeth, mouth, and face health of 25 people with Mowat-Wilson syndrome, a rare genetic condition. Researchers will check for cavities, gum disease, and facial features, and ask about quality of life. No treatment is given—the goal is to gather information t…
Sponsor: University of Milan • Aim: Knowledge-focused
Last updated Jun 27, 2026 12:00 UTC