Radial neuropathy

disease
On this page

Also known as peripheral neuropathy of radial nerveradial nerve peripheral neuropathy

Summary

Radial neuropathy (MONDO:0001459) is a disease and 3 clinical trials. A subtype of mononeuropathy — broader associated-gene and molecular evidence is on the parent page (see Disease family below).

At a glance

  • Clinical trials: 3

Clinical features

No curated clinical features (Orphanet) for this disease.

Identifiers

Disease identifiers

FieldValue
Canonical nameradial neuropathy
Mondo IDMONDO:0001459
MeSHD020425
DOIDDOID:12171
SNOMED CT16644004
UMLSC0748226
MedGen148185
GARD0022947
Anatomy (UBERON)UBERON:0001492
Is cancer (heuristic)no

Also known as: peripheral neuropathy of radial nerve · radial nerve peripheral neuropathy

Disease family

This is a subtype of mononeuropathy. Genetic, therapeutic, and trial evidence is largely curated at the broader-term level — see the parent page for the associated-gene cohort and molecular evidence.

Classification path: disease › human disease › disease by body system or component › nervous system disorderperipheral nervous system disorderperipheral neuropathymononeuropathyradial neuropathy

Related subtypes (6): mononeuritis simplex, peroneal neuropathy, femoral neuropathy, sciatic neuropathy, tibial neuropathy, ulnar neuropathy

Subtypes (1): radial nerve lesion

Genetics & variants

GWAS landscape

No GWAS associations recorded — common-variant (GWAS) studies don’t cover this disease (typical for Mendelian / rare diseases). See the curated gene cohort and Mendelian overlap below.

Variant details and genetic-evidence tiers

No tiered GWAS variants or ClinVar records for this disease.

Genes & proteins

No associated-gene cohort resolved for this disease. Atlas builds the molecular and therapeutic sections — associated genes, protein families, druggability, pathways, interactions, and drug associations — by aggregating over a disease’s associated genes (resolved via GWAS / GenCC / ClinVar / CIViC), and none resolved here. This is expected for antibody-mediated, autoimmune, or otherwise non-gene-defined conditions; the curated evidence for this disease is its clinical features, GWAS susceptibility, and clinical trials (above).

Function

No pathway enrichment — requires an associated-gene cohort.

Therapeutics

No druggable-target or therapeutic data for this disease’s cohort.

Clinical trials & evidence

Clinical trials

Clinical trials: 3.

Phase distribution (across all retrieved trials)

PhaseTrials
Not specified3

Top trials by phase / activity

NCTPhaseStatusTitle
NCT01394822Not specifiedCOMPLETEDNeuromuscular Ultrasound for Focal Neuropathies
NCT05650970Not specifiedCOMPLETEDRadial Nerve Mobilization in Hand Thumb Osteoarthritis Patients
NCT06980779Not specifiedCOMPLETEDThe Correlation of Clinical and Ultrasonographic Findings in Dorsoradial Wrist Pain Patients: Cross Sectional Study

No linked Atlas pages yet — the cross-entity mesh grows as the corpus expands.