Peroneal neuropathy

Summary

Peroneal neuropathy (MONDO:0002910) 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

Field	Value
Canonical name	peroneal neuropathy
Mondo ID	MONDO:0002910
MeSH	D020427
DOID	DOID:4201
NCIT	C27596
UMLS	C0747533
MedGen	148182
GARD	0023296
Is cancer (heuristic)	no

Also known as: peroneal 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 disorder › peripheral nervous system disorder › peripheral neuropathy › mononeuropathy › peroneal neuropathy

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

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)

Phase	Trials
Not specified	3

Top trials by phase / activity

NCT	Phase	Status	Title
NCT01394822	Not specified	COMPLETED	Neuromuscular Ultrasound for Focal Neuropathies
NCT03560505	Not specified	COMPLETED	High-resolution Ultrasound in Lower Extremity Nerves and Common Fibular Neuropathies.
NCT07191301	Not specified	COMPLETED	Functional Strength Training and Kinesiotaping, With and Without Proprioceptive Neuromuscular Facilitation in Fibular (Peroneal) Neuropathy