Cure My Disease

Don't miss your cure!

Log in / Sign up

Peroxisome biogenesis disorder due to PEX11B defect

MONDO:0100279

Any peroxisome biogenesis disorder in which the cause of the disease is a mutation in the PEX11B gene.

Also known as: PEX11B related peroxisome biogenesis disorder, peroxisome biogenesis disorder due to PEX11B defect

7 clinical trials for this condition and its sub-types, 0 tagged with Peroxisome biogenesis disorder due to PEX11B defect itself.

Follow this condition to get notified about new trials

Where it sits in the disease tree

Browse by category →

Part of

↑ Zellweger spectrum disorders (7)

Sub-types of Peroxisome biogenesis disorder due to PEX11B defect

Peroxisome biogenesis disorder 14B 0 trials

Including sub-types (7) Tagged with Peroxisome biogenesis disorder due to PEX11B 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