RareTrial

Rare condition

Hereditary sensory and autonomic neuropathy type 2

ORPHA:970 ↗Gene SCN9AGene WNK1Gene RETREG1Gene KIF1A
Search all Hereditary sensory and autonomic neuropathy type 2 trialsAlert me when a trial opens

6

studies recruiting now

as of 7 Sept 2026

23

studies registered in total

as of 7 Sept 2026

2

countries with a recruiting site

as of 7 Sept 2026

6 Aug 2026

most recent study posted

among recruiting studies

Recruiting trials

Showing the 5 most recently updated recruiting studies, as recorded 7 Sept 2026. Live status on each study page.

See all 6 recruiting studies

Where recruiting studies are running

Countries with at least one recruiting site among the studies above, 7 Sept 2026. Tap a country to search trials there.

ChinaUnited States

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Patient organisations

We do not yet list a dedicated organisation for this condition. The directories below are the best route.

NORD ↗GARD ↗Orphanet ORPHA:970 ↗

About Hereditary sensory and autonomic neuropathy type 2

RareTrial does not yet hold a plain-language description of this condition. The most reliable starting point is Orphanet’s expert page, which lists specialist centres, registries and patient organisations, and the genes involved (SCN9A, WNK1, RETREG1, KIF1A).

Orphanet expert page ↗GARD (NIH) ↗

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Information, not medical advice. Trial listings are shown as recorded on ClinicalTrials.gov; whether any study is right for you is a decision for you and your clinicians, and eligibility is decided by each research team. Disease information from Orphanet (CC BY 4.0).