Rare diseases · Sign or symptom
Tubulointerstitial nephritis
HP:0001970
What it means
A form of inflammation of the kidney affecting the interstitium of the kidneys surrounding the tubules.
Rare diseases that can present with this25
Common30–79%
5Sometimes5–29%
11- Carnitine palmitoyltransferase II deficiency
- Carnitine palmitoyl transferase II deficiency, myopathic form
- Carnitine palmitoyl transferase II deficiency, neonatal form
- Craniofacial dysplasia-short stature-ectodermal anomalies-intellectual disability syndrome
- Drug reaction with eosinophilia and systemic symptoms
- Immune dysregulation-polyendocrinopathy-enteropathy-X-linked syndrome
- Lymphedema-distichiasis syndrome
- Lysinuric protein intolerance
and 3 more in this range
The range is how often this sign appears among people diagnosed with each disease — it is not a probability of having any of them. Many of these signs also occur in common, non-rare conditions. A sign on this page is a conversation to have with a clinician, not a conclusion.
Part of the broader category
Also called: Interstitial nephritis · Nephritis, Tubulointerstitial
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Start free with EleplanThis page uses the Human Phenotype Ontology (2026-06-23) — Human Phenotype Ontology Consortium, hpo.jax.org. Disease associations from Orphanet (INSERM), CC BY 4.0. Content is educational and is not medical advice.