Disease Directory Lysinuric protein intolerance
Rare Disease

Lysinuric protein intolerance

Type

Disease

Gene

SLC7A7

About Lysinuric protein intolerance

Lysinuric protein intolerance is a rare disease catalogued by Orphanet (ORPHA:470). It is associated with the SLC7A7 gene. Search below for active recruiting clinical trials from ClinicalTrials.gov, or visit the Orphanet expert page for specialist centres, natural history studies, and patient registries.

Clinical Trial Eligibility Tips

What to know before applying to Lysinuric protein intolerance trials.

Search ClinicalTrials.gov for "Lysinuric protein intolerance" or filter by Orphanet code ORPHA:470 to find disease-specific studies.

Ask your specialist to refer you to a Centre of Expertise — Orphanet lists all accredited centres for this condition worldwide.

Natural history studies and patient registries often enrol before drug trials open — contact the Orphanet patient community first.

Patient Resources

Patient Organization

Orphanet

Visit website ↗

Orphanet

European reference resource for rare diseases (ORPHA:470)

View on Orphanet ↗

NORD

National Organization for Rare Disorders

Search NORD ↗

Find recruiting Lysinuric protein intolerance trials

Search 500,000+ studies from ClinicalTrials.gov, filtered for Lysinuric protein intolerance. Updated daily.