About Temperature-sensitive oculocutaneous albinism type 1
Temperature-sensitive oculocutaneous albinism type 1 is a rare disease catalogued by Orphanet (ORPHA:352737). It is associated with the TYR 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 Temperature-sensitive oculocutaneous albinism type 1 trials.
Search ClinicalTrials.gov for "Temperature-sensitive oculocutaneous albinism type 1" or filter by Orphanet code ORPHA:352737 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
Find recruiting Temperature-sensitive oculocutaneous albinism type 1 trials
Search 500,000+ studies from ClinicalTrials.gov, filtered for Temperature-sensitive oculocutaneous albinism type 1. Updated daily.