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tubulointerstitial nephritis and uveitis syndrome - Clinical Profile, Genes & Research | Kisho | Kisho

Rare Disease

tubulointerstitial nephritis and uveitis syndrome

MONDO:0011885

Also known as:Dobrin syndromeTINU syndromeTubulointerstitial nephritis and uveitis

Overview

An autoimmune disorder comprising tubulointerstitial nephritis and uveitis.

Diagnosis

Biomarker and diagnostic research for tubulointerstitial nephritis and uveitis syndrome has been reported in the published literature.

Prognosis

Estimated prevalence: Unknown (Unknown prevalence).

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 tubulointerstitial nephritis and uveitis syndrome.

34 publications have been identified in PubMed for tubulointerstitial nephritis and uveitis syndrome. Research spans Case Report / Case Series (53%), Review / Meta-Analysis (29%), and Epidemiology / Natural History (9%).

Research Type	Count	% of Total
Patient case studies	18	53%

Data assembled from 4 of 12 sources · Last updated Sep 20, 2026, 8:43 AM UTC

MONDOHPOClinicalTrials.govFDAPubMedHGNCClinVarClinGenGeneReviewsOrphanetOMIMRUSP

Medical References

External Resources

OMIM

Online Mendelian Inheritance in Man

OMIM:607665

Orphanet

European rare disease database

Orphanet:91500

GARD

Genetic and Rare Diseases Info Center

GARD:9252

Questions for Your Care Team

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tubulointerstitial nephritis and uveitis syndrome

Overview

Diagnosis

Prognosis

Research Landscape

Medical References

External Resources

OMIM

Orphanet

GARD

Related Diseases

Questions for Your Care Team

Questions for Your Care Team

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