Nemaline myopathy 5
MONDO:0011539Amish nemaline myopathy is a type of nemaline myopathy (NM) only observed in several families of the Amish community.
Also known as: ANM, Amish nemaline myopathy, NEM5, TNNT1 nemaline myopathy, nemaline myopathy 5, nemaline myopathy caused by mutation in TNNT1, nemaline myopathy type 5, nemaline myopathy, Amish type
6 clinical trials for this condition and its sub-types, 2 tagged with Nemaline myopathy 5 itself.
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Global study tracks rare muscle disease to pave way for future treatments
Knowledge-focused Recruiting nowThis study follows children and adults worldwide who have a rare genetic muscle disease called TNNT1 myopathy. Researchers aim to document how the disease progresses over time, including survival and motor milestones. The goal is to identify reliable measures that can be used in …
Sponsor: Clinic for Special Children • Aim: Knowledge-focused
Last updated Jun 27, 2026 14:01 UTC
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Spanish study tracks rare muscle disease to speed future treatments
Knowledge-focused Recruiting nowThis study follows 100 people in Spain with nemaline myopathy, a rare muscle disease, to see how their symptoms change over time. Researchers will use ultrasound, movement tests, and breathing checks to map the disease's natural course. The goal is to build a detailed patient dat…
Sponsor: Hospital Universitari Vall d'Hebron Research Institute • Aim: Knowledge-focused
Last updated Jun 27, 2026 12:00 UTC