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autoimmune polyendocrinopathy (APS) - Clinical Profile, Genes & Research | Kisho | Kisho

Rare Disease

autoimmune polyendocrinopathy

MONDO:0017278

Also known as:APSAntiphospholipid SyndromeLloyd's syndrome

Find Clinical TrialsTrials

Overview

A group of diverse conditions that are characterized by spontaneous, multi-organ autoimmunity, which target both endocrine (adrenal, gonad, pancreatic islet cells, parathyroid, pituitary, thyroid) and non-endocrine (gastrointestinal, integumentary, lymphatic) tissues.

OnsetCHILDHOOD

Clinical Trials5 registered · 2 recruiting

Diagnosis

Biomarker and diagnostic research for autoimmune polyendocrinopathy 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.

5 clinical trials registered, 2 recruiting. Interventions under study include drug therapy and other interventions. Pipeline includes 2 PHASE2, 2 NA. Research is primarily sponsored by academic and government institutions.

NCT ID	Title	Phase	Sponsor	Status
[NCT05578105](https://clinicaltrials.gov/study/NCT05578105)

Data assembled from 4 of 12 sources · Last updated Sep 19, 2026, 1:53 PM UTC

MONDOHPOClinicalTrials.govFDAPubMedHGNCClinVarClinGenGeneReviewsOrphanetOMIMRUSP

Medical References

External Resources

Orphanet

European rare disease database

Orphanet:282196

GARD

Genetic and Rare Diseases Info Center

GARD:21116

Questions for Your Care Team

→Are any of the 5 active clinical trials a good fit for my situation?
→Are there specialists or centers of excellence for this condition in my area?
→Is there a patient registry I should consider joining?

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Research Type	Count	% of Total
Research summaries	94	37%
Patient case studies	55	21%
Laboratory research	43	17%
Disease patterns and progression	30	12%
Testing and diagnosis research	13	5%
New treatment approaches	9	4%
Clinical study results	8	3%
Other research	5	2%

autoimmune polyendocrinopathy

Overview

Diagnosis

Research Landscape

Medical References

External Resources

Orphanet

GARD

Subtypes

Related Diseases

Questions for Your Care Team

Questions for Your Care Team

Recent Publications