Disease Directory HSD10 disease, infantile type
Rare Disease

HSD10 disease, infantile type

Type

Clinical subtype

Gene

HSD17B10

About HSD10 disease, infantile type

HSD10 disease, infantile type is a rare disease catalogued by Orphanet (ORPHA:391428). It is associated with the HSD17B10 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 HSD10 disease, infantile type trials.

Search ClinicalTrials.gov for "HSD10 disease, infantile type" or filter by Orphanet code ORPHA:391428 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:391428)

View on Orphanet ↗

NORD

National Organization for Rare Disorders

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Find recruiting HSD10 disease, infantile type trials

Search 500,000+ studies from ClinicalTrials.gov, filtered for HSD10 disease, infantile type. Updated daily.