Tubulointerstitial fibrosis
Symptom Information:
Symptom ID: | HPO:0005576 | |||
Synonyms: |
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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 fibrosis(HPO:0005576) MedDRA: |
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Database Frequency: | 32 / 7739 | |||
Resource: |
All diseases associated with this symptom:
Alström syndrome | (Orphanet:64) |
Autosomal dominant medullary cystic kidney disease with or without hyperuricemia | (Orphanet:34149) |
Autosomal recessive medullary cystic kidney disease | (Orphanet:655) |
Autosomal recessive polycystic kidney disease | (Orphanet:731) |
Chronic respiratory distress with surfactant metabolism deficiency | (Orphanet:217566) |
Dent disease type 1 | (Orphanet:93622) |
Desquamative interstitial pneumonia | (Orphanet:98852) |
Fabry disease | (Orphanet:324) |
Familial idiopathic steroid-resistant nephrotic syndrome with diffuse mesangial proliferation | (Orphanet:93214) |
GAPO syndrome | (Orphanet:2067) |
Glycogen storage disease due to glycogen branching enzyme deficiency, progressive hepatic form | (Orphanet:308621) |
Hypertrophic cardiomyopathy and renal tubular disease due to mitochondrial DNA mutation | (Orphanet:324525) |
Hyperuricemia - anemia - renal failure | (Orphanet:217330) |
Infantile Bartter syndrome with deafness | (Orphanet:89938) |
Joubert syndrome with oculorenal defect | (Orphanet:2318) |
MEDULLARY CYSTIC KIDNEY DISEASE 1 | (OMIM:174000) |
NEPHROLITHIASIS, X-LINKED RECESSIVE, WITH RENAL FAILURE | (OMIM:310468) |
Nephronophthisis 1 | (OMIM:256100) |
Nephronophthisis 12 | (OMIM:613820) |
Nephronophthisis 13 | (OMIM:614377) |
Nephronophthisis 18 | (OMIM:615862) |
Nephronophthisis 19 | (OMIM:616217) |
Nephronophthisis 2 | (OMIM:602088) |
Nephronophthisis 3 | (OMIM:604387) |
Nephronophthisis 4 | (OMIM:606966) |
Nephronophthisis 9 | (OMIM:613824) |
Nephronophthisis-like nephropathy 1 | (OMIM:613159) |
Proximal renal tubular acidosis | (Orphanet:47159) |
Renal cysts and diabetes syndrome | (Orphanet:93111) |
SPONDYLOENCHONDRODYSPLASIA WITH IMMUNE DYSREGULATION | (OMIM:607944) |
Senior-Loken syndrome 6 | (OMIM:610189) |
Tyrosinemia type 1 | (Orphanet:882) |