Micronodular cirrhosis
Symptom Information:
Symptom ID: | HPO:0001413 | |||
Synonyms: |
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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) Cirrhosis(HPO:0001394) Micronodular cirrhosis(HPO:0001413) MedDRA: |
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Database Frequency: | 11 / 7739 | |||
Resource: |
All diseases associated with this symptom:
Alpers syndrome | (Orphanet:726) |
CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIl | (OMIM:614576) |
Cerebroretinal vasculopathy | (Orphanet:3421) |
HERNS syndrome | (Orphanet:63261) |
Hemochromatosis, type 2A | (OMIM:602390) |
Hepatocellular carcinoma | (Orphanet:88673) |
Hereditary vascular retinopathy | (Orphanet:71291) |
Idiopathic copper-associated cirrhosis | (Orphanet:209919) |
Mitochondrial DNA depletion syndrome, hepatocerebral form due to DGUOK deficiency | (Orphanet:279934) |
Retinal vasculopathy and cerebral leukodystrophy | (Orphanet:247691) |
Zellweger-like syndrome without peroxisomal anomalies | (Orphanet:50812) |