Motor peripheral neuropathy

MONDO:0002316

Inflammation or degeneration of the peripheral motor nerves.

Also known as: peripheral motor neuropathy, HSMN, HSMN - hereditary sensory and motor neuropathy, hereditary motor and sensory neuropathy, neuropathic muscular atrophy

6 clinical trials for this condition and its sub-types, 0 tagged with Motor peripheral neuropathy itself.

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Where it sits in the disease tree

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↑ Peripheral neuropathy (1469)

Sub-types of Motor peripheral neuropathy

Charcot-Marie-Tooth disease axonal type 2C 1 trial
Charcot-Marie-Tooth disease type 4G 0 trials
Charcot-Marie-Tooth disease type 5 0 trials
Glossopharyngeal motor neuropathy 0 trials
Hereditary motor and sensory neuropathy, Okinawa type 0 trials
1 sub-type
- Autosomal dominant Charcot-Marie-Tooth disease type 2 due to TFG mutation 0 trials
Motor nerve neuritis 0 trials
1 sub-type
- Asymmetric motor neuropathy 0 trials
Neuropathy, hereditary motor and sensory, type 6A 0 trials
Neuropathy, hereditary motor and sensory, type 6B 0 trials
Peripheral motor neuropathy, childhood-onset, biotin-responsive 0 trials

Including sub-types (6) Tagged with Motor peripheral neuropathy (0)

Trials to join now! 4 Completed 1 Terminated 1

Could a simple blood test track nerve damage? a study investigates NT-3 levels in neuropathy.

Knowledge-focused Stopped early

This study measures levels of a protein called NT-3 in the blood of people with peripheral neuropathy or Charcot-Marie-Tooth disease. Researchers will compare these levels with measures of muscle strength, mobility, and daily function. The goal is to see whether NT-3 levels corre…

Sponsor: Zarife Sahenk • Aim: Knowledge-focused

Last updated Jul 31, 2026 00:00 UTC

Motor peripheral neuropathy

Where it sits in the disease tree

Could a simple blood test track nerve damage? a study investigates NT-3 levels in neuropathy.