Neuronopathy, distal hereditary motor, type 2B

MONDO:0012080

Any neuronopathy, distal hereditary motor in which the cause of the disease is a mutation in the HSPB1 gene.

Also known as: HSPB1 neuronopathy, distal hereditary motor, neuronopathy, distal hereditary motor caused by mutation in HSPB1, HMN 2B, HMN2B, neuronopathy, distal hereditary motor, type IIB, neuropathy, distal hereditary motor, type 2B

15 clinical trials for this condition and its sub-types, 0 tagged with Neuronopathy, distal hereditary motor, type 2B itself.

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Where it sits in the disease tree

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↑ Distal hereditary motor neuropathy type 2 (0)

Including sub-types (15) Tagged with Neuronopathy, distal hereditary motor, type 2B (0)

Trials to join now! 10 Not yet finished but already full! 3 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

Neuronopathy, distal hereditary motor, type 2B

Where it sits in the disease tree

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