Tubulointerstitial fibrosis

Symptom Information:

Symptom ID: HPO:0005576
Synonyms:
Renal interstitial fibrosis [HPO:0005576]
Renal interstitial fibrosis [OMIM:Renal interstitial fibrosis]
Tubulointerstitial fibrosis [OMIM:Tubulointerstitial fibrosis]
Quality:
Cross references:
OMIM: "Renal interstitial fibrosis" [OMIM:Renal interstitial fibrosis]
OMIM: "Tubulointerstitial fibrosis" [OMIM:Tubulointerstitial fibrosis]
Is a (Direct Parents):
HPO         Tubulointerstitial abnormality
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:
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)