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peroxisome biogenesis disorder due to PEX11B defect - Clinical Profile, Genes & Research | Kisho | Kisho

Rare Disease

peroxisome biogenesis disorder due to PEX11B defect

MONDO:0100279

Also known as:PEX11B related peroxisome biogenesis disorder

Overview

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

ResearchLimited published research (4 articles)

Research Landscape

Sourced from ClinicalTrials.gov and PubMed. Publication types are classified using NLM-curated article metadata; research type breakdowns reflect the nature of published work for this disease.

No clinical trials have been registered for peroxisome biogenesis disorder due to PEX11B defect.

4 publications have been identified in PubMed for peroxisome biogenesis disorder due to PEX11B defect. Research spans Basic Science / Preclinical (75%) and Review / Meta-Analysis (25%).

Recent Publications

Vercaemst A (2026). [PMID: 41677620](https://pubmed.ncbi.nlm.nih.gov/41677620/). *Cells*. [Review / Meta-Analysis]
Yang YM (2025). [PMID: 39934809](https://pubmed.ncbi.nlm.nih.gov/39934809/). *J Biomed Sci*. [Basic Science / Preclinical]
Borisyuk A (2025). [PMID: 40689797](https://pubmed.ncbi.nlm.nih.gov/40689797/). *J Cell Biol*. [Basic Science / Preclinical]
Colasante C (2024). [PMID: 39652567](https://pubmed.ncbi.nlm.nih.gov/39652567/). *PLoS One*. [Basic Science / Preclinical]

Data assembled from 2 of 12 sources · Last updated Sep 19, 2026, 4:33 PM UTC

MONDOHPOClinicalTrials.govFDAPubMedHGNCClinVarClinGenGeneReviewsOrphanetOMIMRUSP

Medical References

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peroxisome biogenesis disorder due to PEX11B defect

Overview

Research Landscape

Recent Publications

Medical References

Subtypes

Related Diseases

Questions for Your Care Team

Questions for Your Care Team