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peroxisome biogenesis disorder due to PEX5 defect in the PEX7-binding domain - Clinical Profile, Genes & Research | Kisho | Kisho

Rare Disease

peroxisome biogenesis disorder due to PEX5 defect in the PEX7-binding domain

MONDO:0100265

Overview

Any peroxisome biogenesis disorder due to PEX5 in which the cause of the disease is a mutation in the PEX7-binding domain of the PEX5 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 PEX5 defect in the PEX7-binding domain.

4 publications have been identified in PubMed for peroxisome biogenesis disorder due to PEX5 defect in the PEX7-binding domain. Research spans Basic Science / Preclinical (100%).

Recent Publications

Chen WW (2025). [PMID: 40739340](https://pubmed.ncbi.nlm.nih.gov/40739340/). *Nature cell biology*. [Basic Science / Preclinical]
Jiang CS (2025). [PMID: 39851575](https://pubmed.ncbi.nlm.nih.gov/39851575/). *Cells*. [Basic Science / Preclinical]
Buck GC (2025). [PMID: 40577590](https://pubmed.ncbi.nlm.nih.gov/40577590/). *The Plant cell*. [Basic Science / Preclinical]
Bajdzienko J (2024). [PMID: 38752931](https://pubmed.ncbi.nlm.nih.gov/38752931/). *Journal of cell science*. [Basic Science / Preclinical]

Data assembled from 2 of 12 sources · Last updated Sep 20, 2026, 6:09 PM UTC

MONDOHPOClinicalTrials.govFDAPubMedHGNCClinVarClinGenGeneReviewsOrphanetOMIMRUSP

Medical References

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peroxisome biogenesis disorder due to PEX5 defect in the PEX7-binding domain

Overview

Research Landscape

Recent Publications

Medical References

Subtypes

Related Diseases

Questions for Your Care Team

Questions for Your Care Team