Portal fibrosis
Symptom Information:
Symptom ID: | HPO:0006580 | ||
Synonyms: |
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Quality: | |||
Cross references: |
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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 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: |
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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) |