FPDMM

Clinical trials for FPDMM explained in plain language.

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Trials to join now! 1

Scientists track rare blood disease across generations to unlock cancer clues

Knowledge-focused Recruiting now

This study aims to learn more about a rare, inherited blood disorder called FPDMM, which is caused by a change in the RUNX1 gene. Researchers will follow people with this gene change and their family members over many years to understand how the disease develops, why some people …

Matched conditions: FPDMM

Sponsor: National Human Genome Research Institute (NHGRI) • Aim: Knowledge-focused

Last updated Apr 01, 2026 22:56 UTC

FPDMM

Get alerted when new FPDMM trials appear

Scientists track rare blood disease across generations to unlock cancer clues