X-linked syndromic intellectual disability
MONDO:0020119A syndromic intellectual disability with an X-linked mode of inheritance.
Also known as: X-linked syndromic intellectual disability, intellectual disability, X-linked syndromic, mental retardation, X-linked syndromic, syndromic X-linked intellectual disability, syndromic intellectual disability, X-linked
12 clinical trials for this condition and its sub-types, 0 tagged with X-linked 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 X-linked syndromic intellectual disability
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Allan-Herndon-Dudley syndrome 6 trials
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1 sub-type
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MEHMO syndrome 1 trial
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ATP6AP2-related disorder 0 trials
2 sub-types
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ATR-X-related syndrome 0 trials
2 sub-types
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Borjeson-Forssman-Lehmann syndrome 0 trials
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CASK-related intellectual disability 0 trials
3 sub-types
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Coffin-Lowry syndrome 0 trials
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3 sub-types
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NAA10-related syndrome 0 trials
2 sub-types
- Ogden syndrome 0 trials
- Microphthalmia, syndromic 1 0 trials
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Paganini-Miozzo syndrome 0 trials
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Partington syndrome 0 trials
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Prieto syndrome 0 trials
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Renpenning syndrome 0 trials
4 sub-types
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Wilson-Turner syndrome 0 trials
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1 sub-type
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4 sub-types
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Fried syndrome 0 trials
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Intellectual disability, X-linked 49 0 trials
Most studied deeper sub-types
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MCT8 deficiency drug withdrawal trial raises questions about lifelong treatment
Disease control CompletedThis phase 3 study looked at what happens when males with MCT8 deficiency (a rare genetic condition affecting thyroid hormone transport) stop taking tiratricol. Twenty participants who had been stable on tiratricol were randomly assigned to either continue the drug or receive a p…
Phase 3 • Sponsor: Rare Thyroid Therapeutics International AB • Aim: Disease control
Last updated Jun 27, 2026 12:05 UTC
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Could a single DNA test solve the mystery of rare brain diseases in kids?
Knowledge-focused CompletedThis study looked at whether whole genome sequencing (a complete read of a person's DNA) can help diagnose leukodystrophies, a group of rare brain diseases that are hard to identify. Researchers enrolled 236 children with white matter abnormalities on brain scans but no known gen…
Sponsor: Children's Hospital of Philadelphia • Aim: Knowledge-focused
Last updated Jun 27, 2026 07:56 UTC