Micronodular cirrhosis

Symptom Information:

Symptom ID: HPO:0001413
Synonyms:
Micronodular cirrhosis [OMIM:Micronodular cirrhosis]
Micronodular cirrhosis (1 patient) [OMIM:Micronodular cirrhosis (1 patient)]
Micronodular cirrhosis (less common) [OMIM:Micronodular cirrhosis (less common)]
Quality:
Cross references:
OMIM: "Micronodular cirrhosis" [OMIM:Micronodular cirrhosis]
OMIM: "Micronodular cirrhosis (1 patient)" [OMIM:Micronodular cirrhosis (1 patient)]
OMIM: "Micronodular cirrhosis (less common)" [OMIM:Micronodular cirrhosis (less common)]
Is a (Direct Parents):
HPO         Cirrhosis
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:
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)