Interstitial fibrosis

Symptom Information:

Symptom ID: OMIM : No Id available
Synonyms:
Quality:
Cross references:
OMIM: "Interstitial fibrosis" [OMIM:Interstitial fibrosis]
Is a (Direct Parents):
Is a (Whole tree): HPO:
MedDRA:
Database Frequency: 24 / 7739
Resource:

All diseases associated with this symptom:

ARIMA SYNDROME (OMIM:243910)
Autosomal recessive polycystic kidney disease (Orphanet:731)
Cardiomyopathy, dilated, 1AA with or without left ventricular noncompaction (OMIM:612158)
Cardiomyopathy, dilated, 1P (OMIM:609909)
Cardiomyopathy, dilated, 1Z (OMIM:611879)
Cardiomyopathy, familial hypertrophic, 15 (OMIM:613255)
Cardiomyopathy, familial hypertrophic, 21 (OMIM:614676)
Cardiomyopathy, familial hypertrophic, 7 (OMIM:613690)
Cardiomyopathy, familial restrictive, 3 (OMIM:612422)
Cardiomyopathy, hypertrophic, 25 (OMIM:607487)
Chronic respiratory distress with surfactant metabolism deficiency (Orphanet:217566)
Congenital nephrotic syndrome, Finnish type (Orphanet:839)
Early-onset myopathy with fatal cardiomyopathy (Orphanet:289377)
Hyperuricemia - anemia - renal failure (Orphanet:217330)
INTERSTITIAL NEPHRITIS, KARYOMEGALIC (OMIM:614817)
NEPHROLITHIASIS, X-LINKED RECESSIVE, WITH RENAL FAILURE (OMIM:310468)
Nephronophthisis 1 (OMIM:256100)
Nephronophthisis 13 (OMIM:614377)
Nephronophthisis 3 (OMIM:604387)
Nephronophthisis-like nephropathy 1 (OMIM:613159)
Renal cysts and diabetes syndrome (Orphanet:93111)
SPONDYLOENCHONDRODYSPLASIA WITH IMMUNE DYSREGULATION (OMIM:607944)
SURFACTANT METABOLISM DYSFUNCTION, PULMONARY, 1 (OMIM:265120)
Senior-Boichis syndrome (Orphanet:84081)