Syndromic intellectual disability
MONDO:0000508A intellectual disability that is part of a larger syndrome.
Also known as: syndrome associated with intellectual disability, syndromic intellectual disability
38 clinical trials for this condition and its sub-types, 2 tagged with Syndromic intellectual disability itself.
Follow this condition to get notified about new trialsWhere it sits in the disease tree
Browse by category →Sub-types of Syndromic intellectual disability
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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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X-linked syndromic intellectual disability 0 trials · 12 incl. sub-types
81 sub-types
- Allan-Herndon-Dudley syndrome 6 trials
- Syndromic X-linked intellectual disability Lubs type 3 trials Sub-types →
- MEHMO syndrome 1 trial
- Syndromic X-linked intellectual disability 5 1 trial
- Syndromic X-linked intellectual disability Snyder type 1 trial
- ATP6AP2-related disorder 0 trials Sub-types →
- ATR-X-related syndrome 0 trials Sub-types →
- Borjeson-Forssman-Lehmann syndrome 0 trials
- CASK-related intellectual disability 0 trials Sub-types →
- Coffin-Lowry syndrome 0 trials
- MED12-related intellectual disability syndrome 0 trials Sub-types →
- NAA10-related syndrome 0 trials Sub-types →
- Paganini-Miozzo syndrome 0 trials
- Partington syndrome 0 trials
- Prieto syndrome 0 trials
- Renpenning syndrome 0 trials Sub-types →
- SOX3-related X-linked pituitary hormone deficiency with or without intellectual developmental disorder 0 trials
- Wilson-Turner syndrome 0 trials
- X-linked intellectual disability with hypopituitarism 0 trials Sub-types →
- X-linked intellectual disability with isolated growth hormone deficiency 0 trials
- X-linked intellectual disability, Cabezas type 0 trials
- X-linked intellectual disability, Cantagrel type 0 trials
- X-linked intellectual disability, Cilliers type 0 trials
- X-linked intellectual disability, Pai type 0 trials
- X-linked intellectual disability, Schimke type 0 trials
- X-linked intellectual disability, Schutz type 0 trials
- X-linked intellectual disability, Seemanova type 0 trials
- X-linked intellectual disability, Stevenson type 0 trials
- X-linked intellectual disability, Stocco dos Santos type 0 trials
- X-linked intellectual disability, Stoll type 0 trials
- X-linked intellectual disability, van Esch type 0 trials
- X-linked intellectual disability-acromegaly-hyperactivity syndrome 0 trials
- X-linked intellectual disability-ataxia-apraxia syndrome 0 trials
- X-linked intellectual disability-cardiomegaly-congestive heart failure syndrome 0 trials
- X-linked intellectual disability-cerebellar hypoplasia syndrome 0 trials
- X-linked intellectual disability-corpus callosum agenesis-spastic quadriparesis syndrome 0 trials
- X-linked intellectual disability-craniofacioskeletal syndrome 0 trials
- X-linked intellectual disability-cubitus valgus-dysmorphism syndrome 0 trials
- X-linked intellectual disability-epilepsy syndrome 0 trials Sub-types →
- X-linked intellectual disability-epilepsy-progressive joint contractures-dysmorphism syndrome 0 trials
- X-linked intellectual disability-hypogammaglobulinemia-progressive neurological deterioration syndrome 0 trials
- X-linked intellectual disability-hypogonadism-ichthyosis-obesity-short stature syndrome 0 trials
- X-linked intellectual disability-hypotonia-movement disorder syndrome 0 trials
- X-linked intellectual disability-macrocephaly-macroorchidism syndrome 0 trials
- X-linked intellectual disability-plagiocephaly syndrome 0 trials
- X-linked intellectual disability-precocious puberty-obesity syndrome 0 trials
- X-linked intellectual disability-psychosis-macroorchidism syndrome 0 trials
- X-linked intellectual disability-retinitis pigmentosa syndrome 0 trials
- X-linked intellectual disability-seizures-psoriasis syndrome 0 trials
- X-linked intellectual disability-short stature-overweight syndrome 0 trials
- X-linked intellectual disability-spastic quadriparesis syndrome 0 trials
- Corpus callosum agenesis-intellectual disability-coloboma-micrognathia syndrome 0 trials
- Early-onset parkinsonism-intellectual disability syndrome 0 trials
- Fried syndrome 0 trials
- Intellectual developmental disorder, X-linked, syndromic 37 0 trials
- Intellectual developmental disorder, X-linked, syndromic, Hackmann-Di Donato type 0 trials
- Intellectual developmental disorder, X-linked, syndromic, Pilorge type 0 trials
- Intellectual developmental disorder, X-linked, syndromic, with pigmentary mosaicism and coarse facies 0 trials
- Intellectual disability, X-linked 49 0 trials
- Intellectual disability, X-linked 99, syndromic, female-restricted 0 trials
- Intellectual disability, X-linked syndromic, Turner type 0 trials
- Intellectual disability, X-linked, syndromic 33 0 trials
- Intellectual disability, X-linked, syndromic, 35 0 trials
- Intellectual disability, X-linked, syndromic, Bain type 0 trials
- Intellectual disability, X-linked, syndromic, Houge type 0 trials
- Severe X-linked intellectual disability, Gustavson type 0 trials
- Skeletal dysplasia-intellectual disability syndrome 0 trials
- Syndromic X-linked intellectual disability 12 0 trials
- Syndromic X-linked intellectual disability 14 0 trials
- Syndromic X-linked intellectual disability 17 0 trials
- Syndromic X-linked intellectual disability 34 0 trials
- Syndromic X-linked intellectual disability 7 0 trials
- Syndromic X-linked intellectual disability 94 0 trials
- Syndromic X-linked intellectual disability Abidi type 0 trials
- Syndromic X-linked intellectual disability Chudley-Schwartz type 0 trials
- Syndromic X-linked intellectual disability Claes-Jensen type 0 trials
- Syndromic X-linked intellectual disability Nascimento type 0 trials
- Syndromic X-linked intellectual disability Raymond type 0 trials
- Syndromic X-linked intellectual disability Shashi type 0 trials
- Syndromic X-linked intellectual disability Shrimpton type 0 trials
- Syndromic X-linked intellectual disability Siderius type 0 trials
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Smith-Magenis syndrome 5 trials
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Rubinstein-Taybi syndrome 3 trials
3 sub-types
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Autosomal recessive syndromic intellectual disability 0 trials · 1 incl. sub-types
7 sub-types
- Cohen syndrome 1 trial
- Al Kaissi syndrome 0 trials
- Intellectual developmental disorder with dysmorphic facies, seizures, and distal limb anomalies 0 trials
- Intellectual developmental disorder with neuropsychiatric features 0 trials
- Intellectual disability, autosomal recessive 53 0 trials
- Intellectual disability-hypotonia-spasticity-sleep disorder syndrome 0 trials
- Short stature-brachydactyly-obesity-global developmental delay syndrome 0 trials
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Dyneinopathy 0 trials · 1 incl. sub-types
2 sub-types
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2p25.3 microduplication syndrome 0 trials
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3q27.3 microdeletion syndrome 0 trials
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7p22.1 microduplication syndrome 0 trials
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9p13 microdeletion syndrome 0 trials
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9q31.1q31.3 microdeletion syndrome 0 trials
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9q33.3q34.11 microdeletion syndrome 0 trials
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CK syndrome 0 trials
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Intellectual disability, Wolff type 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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Texts and calls could save lives: new study aims to boost baby vaccinations
Prevention Not yet recruitingThis study tests whether sending text messages or voice call reminders with helpful behavior change tips can improve how many babies get their full set of vaccines on time. About 7,800 caregivers of newborns in Bangladesh will be split into three groups: one gets no reminders, on…
Sponsor: Japan Institute for Health Secutiry • Aim: Prevention
Last updated Jun 27, 2026 12:07 UTC
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Can acupuncture needles Kick-Start a paralyzed stomach after cancer surgery?
Symptom relief Not yet recruitingThis study tests whether electroacupuncture (mild electrical pulses through thin needles) can help patients whose stomachs stop working properly after surgery for digestive tract tumors. Seventy-six adults who had such surgery and developed gastroparesis (stomach paralysis) will …
Sponsor: First Teaching Hospital of Tianjin University of Traditional Chinese Medicine • Aim: Symptom relief
Last updated Jun 27, 2026 12:23 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
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New DNA reader could crack unsolved rare disease cases
Knowledge-focused Not yet recruitingThis study tests a new DNA sequencing method that reads long stretches of DNA to find hidden genetic changes causing rare diseases like albinism and intellectual disability. Researchers will analyze stored blood or DNA from 150 patients who haven't gotten a clear diagnosis yet. T…
Sponsor: University Hospital, Bordeaux • Aim: Knowledge-focused
Last updated Jun 27, 2026 09:03 UTC