Intellectual disability, autosomal dominant 13
MONDO:0013805Any autosomal dominant non-syndromic intellectual disability in which the cause of the disease is a mutation in the DYNC1H1 gene.
Also known as: DYNC1H1 autosomal dominant non-syndromic intellectual disability, MRD13, autosomal dominant intellectual disability 13, autosomal dominant non-syndromic intellectual disability caused by mutation in DYNC1H1, intellectual disability, autosomal dominant 13, intellectual disability, autosomal dominant 13, with neuronal migration defects, intellectual disability, autosomal dominant type 13, mental retardation, autosomal dominant type 13
18 clinical trials for this condition and its sub-types.
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VR headsets tested as a possible treatment for blindness
Disease control TerminatedThis study tested whether using a virtual reality headset for one-hour sessions could help regenerate damaged optic nerves and improve vision in people with glaucoma or other retinal diseases. The idea came from promising results in rodents. However, the trial was terminated earl…
Phase: NA • Sponsor: Stanford University • Aim: Disease control
Last updated Jun 27, 2026 08:03 UTC
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New eye scanner software could sharpen diagnosis of macular degeneration
Diagnosis TerminatedThis study tested a new software called AngioScan, used with an already-approved eye camera, to see if it can take better pictures of the back of the eye. Researchers looked at 150 patients with retinal problems like macular degeneration. The goal was to find out if the software …
Sponsor: University of California, Los Angeles • Aim: Diagnosis
Last updated Jun 27, 2026 12:10 UTC