Charcot-Marie-Tooth disease type 2
MONDO:0018993A Charcot-Marie-Tooth disease characterized by abnormalities in the axon of the peripheral nerve cell.
Also known as: CMT2, autosomal dominant axonal Charcot-Marie-Tooth disease, hereditary motor and sensory neuropathy type 2, Charcot-Marie-Tooth type 2, autosomal dominant Charcot-Marie-Tooth disease type 2
16 clinical trials for this condition and its sub-types, 3 tagged with Charcot-Marie-Tooth disease type 2 itself.
Follow this condition to get notified about new trialsWhere it sits in the disease tree
Browse by category →Sub-types of Charcot-Marie-Tooth disease type 2
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Charcot-Marie-Tooth disease type 2A1 2 trials
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Charcot-Marie-Tooth disease type 2A2 2 trials
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Charcot-Marie-Tooth disease type 2D 2 trials
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Charcot-Marie-Tooth disease type 2J 2 trials
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Charcot-Marie-Tooth disease type 2B 0 trials
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Giant axonal neuropathy 2 0 trials
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Global registry aims to map the full course of Charcot-Marie-Tooth disease
Knowledge-focused Recruiting nowResearchers are building a global registry to collect patient-reported surveys, genetic test results, and medical records from people with Charcot-Marie-Tooth disease and related inherited neuropathies. The study is open to children and adults with a confirmed or suspected diagno…
Sponsor: Hereditary Neuropathy Foundation • Aim: Knowledge-focused
Last updated Sep 19, 2026 00:00 UTC
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Wearable tech tracks fatigue in muscle disease patients
Knowledge-focused Recruiting nowThis study aims to find better ways to measure fatigue and walking problems in people with neuromuscular diseases like muscular dystrophy and spinal muscular atrophy. Researchers will use a wearable sensor to track physical activity for one week in daily life and during a walking…
Sponsor: IRCCS Eugenio Medea • Aim: Knowledge-focused
Last updated Jun 27, 2026 08:12 UTC