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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New drug FOG-001 takes on Hard-to-Treat cancers
Disease control Recruiting nowThis early-phase trial is testing a new drug, FOG-001, in about 595 people with advanced or metastatic solid tumors, including colorectal, prostate, and liver cancers. The drug is given alone or with other cancer treatments to see if it is safe and shrinks tumors. The study is cu…
Phase 1/2 • Sponsor: Parabilis Medicines, Inc. • Aim: Disease control
Last updated Aug 19, 2026 00:00 UTC
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Could a common ADHD drug tame attention issues in rare KBG syndrome?
Disease control Recruiting nowThis trial tests whether methylphenidate, a standard ADHD medication, can reduce attention and hyperactivity problems in children and adolescents with KBG syndrome, a rare genetic condition often accompanied by ADHD-like symptoms. Participants receive alternating blocks of the dr…
Phase 4 • Sponsor: Radboud University Medical Center • Aim: Disease control
Last updated Aug 13, 2026 00:00 UTC
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First gene therapy for rare brain disorder begins testing in kids
Disease control Recruiting nowThis early-stage trial tests a gene therapy called Urbagen in 12 children aged 2-12 with CTNNB1 neurodevelopmental syndrome, a rare genetic condition causing motor and cognitive delays. The therapy is given as a single infusion into the brain fluid, along with immunosuppressant d…
Phase 1/2 • Sponsor: CTNNB1 Foundation • Aim: Disease control
Last updated Jun 27, 2026 12:00 UTC
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Could a Parkinson's drug ease symptoms of a rare childhood brain condition?
Symptom relief Recruiting nowThis study tests whether L-dopa, a drug used for Parkinson's, can improve movement and communication in children with a rare genetic disorder called CTNNB1 syndrome. The condition causes developmental delays, muscle stiffness, and trouble walking. Seven children aged 1 to 15 will…
Sponsor: University Hospital, Montpellier • Aim: Symptom relief
Last updated Jun 27, 2026 13:00 UTC
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Mobile pain team brings relief to kids with intellectual disabilities
Symptom relief Recruiting nowThis study tests a mobile team of pain specialists who visit children and young adults (up to age 25) with moderate to severe intellectual disabilities, autism, or multiple disabilities. The team works with families and caregivers to assess and manage pain in the patient's usual …
Sponsor: University Hospital, Brest • Aim: Symptom relief
Last updated Jun 27, 2026 08:07 UTC
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Can mapping rare genetic variants unlock better care for autism-related disorders?
Knowledge-focused Recruiting nowThis international online study collects medical, behavioral, and developmental information from people with rare genetic changes that are linked to autism and other neurodevelopmental disorders. By partnering with families, researchers aim to build a detailed database to improve…
Sponsor: Simons Searchlight • Aim: Knowledge-focused
Last updated Jul 25, 2026 00:00 UTC
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Scientists study rare gene to unravel autism and speech problems
Knowledge-focused Recruiting nowThis study looks at people who have changes in a gene called FOXP1, which can cause developmental delays, speech problems, and autism-like traits. Researchers will use interviews, play-based assessments, and genetic tests to better understand these conditions. The goal is to lear…
Sponsor: Icahn School of Medicine at Mount Sinai • Aim: Knowledge-focused
Last updated Jun 27, 2026 12:38 UTC
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New study aims to decode emotional challenges in intellectual disability
Knowledge-focused Recruiting nowThis study looks at how adults with intellectual developmental disorder (IDD) understand emotions, compared to people without IDD. Researchers will test 60 adults using tasks that involve recognizing facial expressions, emotions in context, and vocal tones. The goal is to find sp…
Sponsor: Hôpital le Vinatier • Aim: Knowledge-focused
Last updated Jun 27, 2026 12:03 UTC
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Researchers launch major study to understand rare childhood epilepsy disorders
Knowledge-focused Recruiting nowThis study tracks children and adults with genetic developmental and epileptic encephalopathy (DEE) over time. It does not test any treatment but collects information on development, seizures, and quality of life through in-person visits, virtual visits, or online surveys. The go…
Sponsor: Weill Medical College of Cornell University • Aim: Knowledge-focused
Last updated Jun 27, 2026 09:06 UTC
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Study aims to uncover hidden mental health struggles in rare genetic disorder
Knowledge-focused Recruiting nowThis study looks at psychiatric symptoms in people with White-Sutton syndrome, a rare genetic condition. Researchers will interview 30 children and adults and use standard questionnaires to identify anxiety, OCD, autism, and other issues. The goal is to better understand these sy…
Sponsor: Centre Hospitalier Universitaire Dijon • Aim: Knowledge-focused
Last updated Jun 27, 2026 09:01 UTC
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Researchers launch registry to unlock secrets of rare genetic disorders
Knowledge-focused Recruiting nowThis study collects information from people with ASXL-related disorders (such as Bohring-Opitz syndrome) to better understand how these conditions progress and are managed. No new treatments are tested; instead, participants share their medical history and records through surveys…
Sponsor: University of California, Los Angeles • Aim: Knowledge-focused
Last updated Jun 27, 2026 08:06 UTC
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Massive study aims to unlock secrets of rare genetic disorders
Knowledge-focused Recruiting nowThis study is collecting blood, tissue, and medical information from up to 1,000 people with RASopathies—a group of genetic conditions that affect development and raise cancer risk. Researchers will store these samples and data in a database for future studies. The goal is to lea…
Sponsor: Children's Hospital Medical Center, Cincinnati • Aim: Knowledge-focused
Last updated Jun 27, 2026 08:05 UTC
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Researchers track rare genetic disorders to prepare for future treatments
Knowledge-focused Recruiting nowThis study is observing 600 people of any age with STXBP1 or SYNGAP1 gene mutations to better understand how these disorders affect development, seizures, and quality of life. No treatment is given; instead, researchers will collect data from routine clinical assessments over tim…
Sponsor: Children's Hospital of Philadelphia • Aim: Knowledge-focused
Last updated Jun 27, 2026 07:55 UTC
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Dragonfly study launches to map rare genetic syndrome
Knowledge-focused Recruiting nowThe Dragonfly study is an international observational project tracking the development of 250 children and adults with CTNNB1 neurodevelopmental syndrome. Researchers will collect medical history, perform neurological exams, and use questionnaires to understand how symptoms and a…
Sponsor: University Medical Centre Ljubljana • Aim: Knowledge-focused
Last updated Jun 27, 2026 07:51 UTC