Tubulointerstitial nephritis

Symptom Information:

Symptom ID: HPO:0001970
Synonyms:
Interstitial nephritis [HPO:0001970]
Nephritis, Tubulointerstitial [HPO:0001970]
Interstitial nephritis [Orphanet:38160]
Interstitial nephritis (disorder) [Orphanet:38160]
Interstitial nephritis (qualifier value) [Orphanet:38160]
Nephritis, Interstitial [Orphanet:38160]
Interstitial nephritis [OMIM:Interstitial nephritis]
Tubulointerstitial nephritis [OMIM:Tubulointerstitial nephritis]
Interstitial nephropathy [Orphanet:38160]
Nephritis interstitial [Orphanet:38160]
Tubulointerstitial nephritis [MedDRA:10048302]
Acute interstitial nephritis [MedDRA:10048302]
Chronic interstitial nephritis [MedDRA:10048302]
Interstitial nephritis acute [MedDRA:10048302]
Interstitial nephritis chronic [MedDRA:10048302]
Nephritis interstitial [MedDRA:10048302]
Nephritis interstitial acute [MedDRA:10048302]
Nephritis interstitial chronic [MedDRA:10048302]
Renal interstitium disorder [MedDRA:10048302]
Renal tubulitis [MedDRA:10048302]
Interstitial nephropathy [OMIM:Interstitial nephropathy]
Quality:
Cross references:
HPO:0008654 "Tubulointerstitial nephropathy" [Orphanet:38160]
Orphanet:38160 "Interstitial nephropathy" [Orphanet:38160]
OMIM: "Interstitial nephritis" [OMIM:Interstitial nephritis]
OMIM: "Tubulointerstitial nephritis" [OMIM:Tubulointerstitial nephritis]
OMIM: "Interstitial nephropathy" [OMIM:Interstitial nephropathy]
UMLS:C0027707 "Nephritis, Interstitial" [Orphanet:38160]
Is a (Direct Parents):
HPO         Tubulointerstitial abnormality
MedDRA Nephritis NEC
Orphanet Nephropathy
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Abnormality of the genitourinary system(HPO:0000119)
          Abnormality of the urinary system(HPO:0000079)
             Abnormality of the upper urinary tract(HPO:0010935)
                Abnormality of the kidney(HPO:0000077)
                   Abnormal renal morphology(HPO:0012210)
                      Abnormality of the nephron(HPO:0012575)
                         Abnormality of the renal tubule(HPO:0000091)
                            Tubulointerstitial abnormality(HPO:0001969)
                               Tubulointerstitial nephritis(HPO:0001970)
MedDRA:
Renal and urinary disorders(MedDRA:10038359)
    Nephropathy(HPO:0000112)
       Nephritis NEC(MedDRA:10029137)
          Tubulointerstitial nephritis(HPO:0001970)
Database Frequency: 27 / 7739
Resource:

All diseases associated with this symptom:

Alström syndrome (Orphanet:64)
Autosomal dominant medullary cystic kidney disease with or without hyperuricemia (Orphanet:34149)
Blau syndrome (Orphanet:90340)
Castleman disease (Orphanet:160)
Cranioectodermal dysplasia (Orphanet:1515)
Cranioectodermal dysplasia 1 (OMIM:218330)
Drug rash with eosinophilia and systemic symptoms (Orphanet:139402)
Eosinophilic granulomatosis with polyangiitis (Orphanet:183)
Fabry disease (Orphanet:324)
HYPERURICEMIC NEPHROPATHY, FAMILIAL JUVENILE, 3 (OMIM:614227)
Hemorrhagic fever - renal syndrome (Orphanet:340)
Hypouricemia, renal, 2 (OMIM:612076)
INTERSTITIAL NEPHRITIS, KARYOMEGALIC (OMIM:614817)
Isolated CoQ-cytochrome C reductase deficiency (Orphanet:1460)
Kawasaki disease (Orphanet:2331)
Lymphedema - distichiasis (Orphanet:33001)
MEDULLARY CYSTIC KIDNEY DISEASE 1 (OMIM:174000)
MELAS (Orphanet:550)
Nephronophthisis 18 (OMIM:615862)
Nephronophthisis 2 (OMIM:602088)
Polyarteritis nodosa, childhood-onset (OMIM:615688)
Renal tubulopathy - encephalopathy - liver failure (Orphanet:254902)
Senior-Loken syndrome 9 (OMIM:616629)
Vitamin B12-unresponsive methylmalonic acidemia (Orphanet:27)
Vitamin B12-unresponsive methylmalonic acidemia type mut- (Orphanet:79312)
Vitamin B12-unresponsive methylmalonic acidemia type mut0 (Orphanet:289916)
Williams syndrome (Orphanet:904)