About Congenital dyserythropoietic anemia type III
Congenital dyserythropoietic anemia type III is a rare disease catalogued by Orphanet (ORPHA:98870). It is associated with the KIF23, RACGAP1 genes. 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 Congenital dyserythropoietic anemia type III trials.
Search ClinicalTrials.gov for "Congenital dyserythropoietic anemia type III" or filter by Orphanet code ORPHA:98870 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 Congenital dyserythropoietic anemia type III trials
Search 500,000+ studies from ClinicalTrials.gov, filtered for Congenital dyserythropoietic anemia type III. Updated daily.