Tubulointerstitial nephritis
Symptom Information:
Symptom ID: | HPO:0001970 | |||||||||||||||||||||
Synonyms: |
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Is a (Direct Parents): |
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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) |
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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) |