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autoimmune polyendocrinopathy type 3 - Clinical Profile, Genes & Research | Kisho | Kisho

Rare Disease

autoimmune polyendocrinopathy type 3

MONDO:0016422

Also known as:APS type 3APS3autoimmune polyendocrine syndrome type 3

Overview

A rare, endocrine disease characterized by autoimmune thyroid disease associated with at least one other autoimmune disease, such as type I diabetes mellitus, chronic atrophic gastritis, pernicious anemia, vitiligo, alopecia, or myasthenia gravis, but excluding Addison disease.

Diagnosis

Biomarker and diagnostic research for autoimmune polyendocrinopathy type 3 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 autoimmune polyendocrinopathy type 3.

32 publications have been identified in PubMed for autoimmune polyendocrinopathy type 3. Research spans Case Report / Case Series (50%), Epidemiology / Natural History (22%), and Review / Meta-Analysis (13%).

Research Type	Count	% of Total
Patient case studies	16	50%

Data assembled from 3 of 12 sources · Last updated Sep 19, 2026, 3:30 AM UTC

MONDOHPOClinicalTrials.govFDAPubMedHGNCClinVarClinGenGeneReviewsOrphanetOMIMRUSP

Medical References

External Resources

Orphanet

European rare disease database

Orphanet:227982

GARD

Genetic and Rare Diseases Info Center

GARD:10980

Questions for Your Care Team

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autoimmune polyendocrinopathy type 3

Overview

Diagnosis

Research Landscape

Medical References

External Resources

Orphanet

GARD

Related Diseases

Questions for Your Care Team

Questions for Your Care Team

Recent Publications