Periportal fibrosis
Symptom Information:
Symptom ID: | HPO:0001405 | ||
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) Hepatic fibrosis(HPO:0001395) Periportal fibrosis(HPO:0001405) MedDRA: |
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Database Frequency: | 5 / 7739 | ||
Resource: |
All diseases associated with this symptom:
Autosomal recessive polycystic kidney disease | (Orphanet:731) |
CEREBELLAR VERMIS APLASIA WITH ASSOCIATED FEATURES SUGGESTING SMITH-LEMLI-OPITZSYNDROME AND MECKEL SYNDROME | (OMIM:213010) |
Hemochromatosis, type 2B | (OMIM:613313) |
Mitochondrial DNA depletion syndrome, hepatocerebral form due to DGUOK deficiency | (Orphanet:279934) |
Short rib-polydactyly syndrome, Beemer-Langer type | (Orphanet:93268) |