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Orphanet Rare Disease Ontology
Last uploaded:
July 3, 2024
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| Preferred Name | Tubulointerstitial nephritis and uveitis syndrome | |
| Synonyms |
TINU syndrome Dobrin syndrome |
|
| Definitions |
A rare renal tubular disease characterized by early-onset tubulointerstitial nephritis associated with anterior uveitis. |
|
| ID |
http://www.orpha.net/ORDO/Orphanet_91500 |
|
| alternative_term |
TINU syndrome Dobrin syndrome
|
|
| definition |
A rare renal tubular disease characterized by early-onset tubulointerstitial nephritis associated with anterior uveitis.
|
|
| definition_citation |
Orphanet
|
|
| expertlink |
https://www.orpha.net/consor/cgi-bin/OC_Exp.php?Lng=en&Expert=91500 |
|
| has_age_of_onset |
Adolescent Adult Childhood Elderly
|
|
| has_inheritance |
Multigenic/multifactorial
|
|
| hasDbXref |
MeSH:C536922 OMIM:607665 MedDRA:10069034 ICD-11:9A96.1 UMLS:C1843273 ICD-10:N10
|
|
| label |
Tubulointerstitial nephritis and uveitis syndrome
|
|
| notation |
ORPHA:91500
|
|
| part_of | ||
| prefixIRI |
ORDO:Orphanet_91500
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|
| prefLabel |
Tubulointerstitial nephritis and uveitis syndrome
|
|
| present_in |
Worldwide AND has_point_prevalence_range : Unknown
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| treeView | ||
| subClassOf |
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