Disease Directory Partial hydatidiform mole
Rare Disease

Partial hydatidiform mole

Type

Clinical subtype

Gene

NLRP7, KHDC3L

About Partial hydatidiform mole

Partial hydatidiform mole is a rare disease catalogued by Orphanet (ORPHA:254693). It is associated with the NLRP7, KHDC3L 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 Partial hydatidiform mole trials.

Search ClinicalTrials.gov for "Partial hydatidiform mole" or filter by Orphanet code ORPHA:254693 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:254693)

View on Orphanet ↗

NORD

National Organization for Rare Disorders

Search NORD ↗

Find recruiting Partial hydatidiform mole trials

Search 500,000+ studies from ClinicalTrials.gov, filtered for Partial hydatidiform mole. Updated daily.