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mononeuritis multiplex - Clinical Profile, Genes & Research | Kisho | Kisho

Rare Disease

mononeuritis multiplex

MONDO:0002128

Overview

A painful asymmetric asynchronous sensory and motor peripheral neuropathy involving isolated damage to at least 2 separate nerve areas; associated with (but not limited to) systemic disorders such as diabetes, vasculitis, amyloidosis, direct tumor involvement, polyarteritis nodosa, rheumatoid arthritis, systemic lupus erythematosus, and paraneoplastic syndromes. It also may be associated with Lyme disease, Wegener's granulomatosis, Sjogren syndrome, cryoglobulinemia, hypereosinophilia, temporal arteritis, scleroderma, sarcoidosis, leprosy, acute viral hepatitis A, and acquired immunodeficiency syndrome.

Diagnosis

Biomarker and diagnostic research for mononeuritis multiplex has been reported in the published literature.

Research Landscape

Sourced from ClinicalTrials.gov and PubMed. Publication types are classified using NLM-curated article metadata; research type breakdowns reflect the nature of published work for this disease.

No clinical trials have been registered for mononeuritis multiplex.

66 publications have been identified in PubMed for mononeuritis multiplex. Research spans Case Report / Case Series (72%), Review / Meta-Analysis (11%), and Epidemiology / Natural History (9%).

Research Type	Count	% of Total
Patient case studies	47	72%

Data assembled from 2 of 12 sources · Last updated Sep 19, 2026, 6:52 PM UTC

MONDOHPOClinicalTrials.govFDAPubMedHGNCClinVarClinGenGeneReviewsOrphanetOMIMRUSP

Medical References

External Resources

GARD

Genetic and Rare Diseases Info Center

GARD:7056

Questions for Your Care Team

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mononeuritis multiplex

Overview

Diagnosis

Research Landscape

Medical References

External Resources

GARD

Related Diseases

Questions for Your Care Team

Questions for Your Care Team

Recent Publications