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Start free with EleplanTubulointerstitial nephritis and uveitis syndrome
ORPHA:91500Disease
Also called Dobrin syndrome · TINU syndrome
What it is
A rare renal tubular disease characterized by early-onset tubulointerstitial nephritis associated with anterior uveitis.
Key facts
- Age of onset
- Adolescent, Adult, Childhood, Elderly
- Inheritance
- Multigenic/multifactorial
- Classified as
- Disease
Signs and symptoms
Very common80–99%
6Common30–79%
13Sometimes5–29%
31- Abdominal pain
- Aminoaciduria
- Anorexia
- Anterior chamber flare
- Arthralgia
- Cataract
- Choroidal neovascularization
- Cystoid macular edema
and 23 more in this range
These ranges are how often a sign appears across everyone diagnosed, not a prediction for one person — most people have some of these and not others. Orphanet also records findings that are specifically absent in this disease; those are in the data but not listed here.
ICD-10 codes
Cross-references
Orphadata Science: Free access data from Orphanet. © INSERM 1999. Data version 2026-06-23. Available under CC BY 4.0. This is a reference, not medical advice.
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