Disease Directory Chronic myelomonocytic leukemia
Blood

Chronic myelomonocytic leukemia

Type

Disease

Gene

ETV6, ASXL1, SRSF2

About Chronic myelomonocytic leukemia

Chronic myelomonocytic leukemia is a rare disease catalogued by Orphanet (ORPHA:98823). It is associated with the ETV6, ASXL1, SRSF2 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 Chronic myelomonocytic leukemia trials.

Search ClinicalTrials.gov for "Chronic myelomonocytic leukemia" or filter by Orphanet code ORPHA:98823 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:98823)

View on Orphanet ↗

NORD

National Organization for Rare Disorders

Search NORD ↗

Find recruiting Chronic myelomonocytic leukemia trials

Search 500,000+ studies from ClinicalTrials.gov, filtered for Chronic myelomonocytic leukemia. Updated daily.