Skip to main content

RareConnect.ioRare Intelligence

Explore Data Discover Patient Groups News Partner

Sign In Sign Up

Explore Data Patient Groups News Partner

RareConnect.ioRare Intelligence

Combining the speed of AI with the wisdom of the community to build the world's most accurate disease registry.

Explore

Disease Directory
Patient Groups
News
FAQ
MONDO Ontology ↗

Get Involved

Partner with Us
Register Your PAG
Community
Pricing

Legal

Privacy Policy
Terms of Service
Accessibility
Contact Us

© 2025 RareConnect.io. Powered by MONDO Ontology

peroxisome biogenesis disorder 10B | RareConnect | RareConnect.io

/peroxisome biogenesis disorder due to PEX3 defect

/peroxisome biogenesis disorder 10B

peroxisome biogenesis disorder 10B

Rare Disease

MONDO:0054549

Also Known As

peroxisome biogenesis disorder 10BPBD10B

Patient-Friendly Information

Comprehensive, easy-to-understand information about this condition

Checking for content...

Associated Genes

Gene data from MyGene.info • Click to view on NCBI Gene

External Resources

OMIM

OMIM:617370 ↗

Related Diseases

peroxisome biogenesis disorder 10A (Zellweger)

MONDO:0013948

← Back to All Diseases