Disease Directory Distal hereditary motor neuropathy, Jerash type
Rare Disease

Distal hereditary motor neuropathy, Jerash type

Type

Disease

Gene

SIGMAR1

About Distal hereditary motor neuropathy, Jerash type

Distal hereditary motor neuropathy, Jerash type is a rare disease catalogued by Orphanet (ORPHA:139552). It is associated with the SIGMAR1 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 Distal hereditary motor neuropathy, Jerash type trials.

Search ClinicalTrials.gov for "Distal hereditary motor neuropathy, Jerash type" or filter by Orphanet code ORPHA:139552 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:139552)

View on Orphanet ↗

NORD

National Organization for Rare Disorders

Search NORD ↗

Find recruiting Distal hereditary motor neuropathy, Jerash type trials

Search 500,000+ studies from ClinicalTrials.gov, filtered for Distal hereditary motor neuropathy, Jerash type. Updated daily.