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single-organ polyarteritis nodosa - Clinical Profile, Genes & Research | Kisho | Kisho

Rare Disease

single-organ polyarteritis nodosa

MONDO:0018595

Also known as:single-organ PANsingle-organ periarteritis nodosa

Overview

Single-organ polyarteritis nodosa (PAN) is a rare, often mild form of PAN characterized by limited disease without generalized manifestations, most often affecting the skin (cutaneous PAN), the brain, eyes, pancreas, testicles, ureter, breasts, or ovaries. Affected patients are often younger than those with systemic PAN and relapses appear to be more common.

Diagnosis

Biomarker and diagnostic research for single-organ polyarteritis nodosa 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 single-organ polyarteritis nodosa.

12 publications have been identified in PubMed for single-organ polyarteritis nodosa. Research spans Epidemiology / Natural History (33%), Diagnostic / Biomarker (17%), and Review / Meta-Analysis (17%).

Research Type	Count	% of Total
Disease patterns and progression	4	33%

Data assembled from 3 of 12 sources · Last updated Sep 19, 2026, 10:42 PM UTC

MONDOHPOClinicalTrials.govFDAPubMedHGNCClinVarClinGenGeneReviewsOrphanetOMIMRUSP

Medical References

External Resources

Orphanet

European rare disease database

Orphanet:439755

GARD

Genetic and Rare Diseases Info Center

GARD:21832

Questions for Your Care Team

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single-organ polyarteritis nodosa

Overview

Diagnosis

Research Landscape

Medical References

External Resources

Orphanet

GARD

Related Diseases

Questions for Your Care Team

Questions for Your Care Team

Recent Publications