Portal fibrosis

Symptom Information:

Symptom ID: HPO:0006580
Synonyms:
PORTAL FIBROSIS SHOWN ON BIOPSY [HPO:0006580]
Portal fibrosis shown on biopsy [OMIM:Portal fibrosis shown on biopsy]
Quality:
Cross references:
OMIM: "Portal fibrosis shown on biopsy" [OMIM:Portal fibrosis shown on biopsy]
Is a (Direct Parents):
HPO         Abnormality of the biliary system
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Abnormality of the abdomen(HPO:0001438)
          Abnormality of the abdominal organs(HPO:0002012)
             Abnormality of the liver(HPO:0001392)
                Abnormality of the biliary system(HPO:0004297)
                   Portal fibrosis(HPO:0006580)
MedDRA:
Database Frequency: 10 / 7739
Resource:

All diseases associated with this symptom:

Biliary atresia (Orphanet:30391)
Early-onset familial noncirrhotic portal hypertension (ORPHA:494348)
Hemochromatosis, type 2A (OMIM:602390)
Hereditary North American Indian childhood cirrhosis (Orphanet:168583)
Hypermethioninemia encephalopathy due to adenosine kinase deficiency (Orphanet:289290)
MERRF (Orphanet:551)
Mitochondrial DNA depletion syndrome, hepatocerebral form due to DGUOK deficiency (Orphanet:279934)
Nephronophthisis 18 (OMIM:615862)
Progressive familial intrahepatic cholestasis type 3 (Orphanet:79305)
Roifman syndrome (Orphanet:353298)