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Peroxisome biogenesis disorder due to PEX10 defect

MONDO:0100264

Any Zellweger spectrum disorder in which the cause of the disease is a mutation in the PEX10 gene.

Also known as: PEX10 related Zellweger spectrum disorder, peroxisome biogenesis disorder due to PEX10 defect

7 clinical trials for this condition and its sub-types, 0 tagged with Peroxisome biogenesis disorder due to PEX10 defect itself.

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↑ Zellweger spectrum disorders (7)

Sub-types of Peroxisome biogenesis disorder due to PEX10 defect

Peroxisome biogenesis disorder 6A (Zellweger) 0 trials
Peroxisome biogenesis disorder 6B 0 trials

Including sub-types (7) Tagged with Peroxisome biogenesis disorder due to PEX10 defect (0)

Trials to join now! 4 Completed 2 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