Disease Directory Isolated bone marrow mastocytosis
Rare Disease

Isolated bone marrow mastocytosis

Type

Disease

Gene

KIT

About Isolated bone marrow mastocytosis

Isolated bone marrow mastocytosis is a rare disease catalogued by Orphanet (ORPHA:158778). It is associated with the KIT 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 Isolated bone marrow mastocytosis trials.

Search ClinicalTrials.gov for "Isolated bone marrow mastocytosis" or filter by Orphanet code ORPHA:158778 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:158778)

View on Orphanet ↗

NORD

National Organization for Rare Disorders

Search NORD ↗

Find recruiting Isolated bone marrow mastocytosis trials

Search 500,000+ studies from ClinicalTrials.gov, filtered for Isolated bone marrow mastocytosis. Updated daily.