Disease Directory Mutilating hereditary sensory neuropathy with spastic paraplegia
Rare Disease

Mutilating hereditary sensory neuropathy with spastic paraplegia

Type

Disease

Gene

CCT5

About Mutilating hereditary sensory neuropathy with spastic paraplegia

Mutilating hereditary sensory neuropathy with spastic paraplegia is a rare disease catalogued by Orphanet (ORPHA:139578). It is associated with the CCT5 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 Mutilating hereditary sensory neuropathy with spastic paraplegia trials.

Search ClinicalTrials.gov for "Mutilating hereditary sensory neuropathy with spastic paraplegia" or filter by Orphanet code ORPHA:139578 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

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Orphanet

European reference resource for rare diseases (ORPHA:139578)

View on Orphanet ↗

NORD

National Organization for Rare Disorders

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Find recruiting Mutilating hereditary sensory neuropathy with spastic paraplegia trials

Search 500,000+ studies from ClinicalTrials.gov, filtered for Mutilating hereditary sensory neuropathy with spastic paraplegia. Updated daily.