Cirrhosis

Symptom Information:

Symptom ID: HPO:0001394
Synonyms:
Hepatic cirrhosis [HPO:0001394]
LIVER CIRRHOSIS [HPO:0001394]
Cirrhosis of liver (disorder) [Orphanet:29120]
Liver Cirrhosis [Orphanet:29120]
Cirrhosis [Orphanet:29120]
Cirrhosis [OMIM:Cirrhosis]
Hepatic cirrhosis [OMIM:Hepatic cirrhosis]
Liver cirrhosis [OMIM:Liver cirrhosis]
Hepatic cirrhosis [Orphanet:29120]
Hepatic cirrhosis [MedDRA:10019641]
Chronic liver disease and cirrhosis [MedDRA:10019641]
Cirrhosis liver [MedDRA:10019641]
Cirrhosis liver postnecrotic [MedDRA:10019641]
Cirrhosis of liver [MedDRA:10019641]
Cirrhosis of liver without mention of alcohol [MedDRA:10019641]
Hepatic cirrhosis NOS [MedDRA:10019641]
Hepatic cirrhosis post necrotic [MedDRA:10019641]
Liver cirrhosis [MedDRA:10019641]
Cirrhosis liver post necrotic [MedDRA:10019641]
Decompensated cirrhosis [MedDRA:10019641]
Compensated cirrhosis [MedDRA:10019641]
Cirrhosis (1 patient) [OMIM:Cirrhosis (1 patient)]
Cirrhosis (in late-onset cases) [OMIM:Cirrhosis (in late-onset cases)]
Cirrhosis (in some patients) [OMIM:Cirrhosis (in some patients)]
Cirrhosis (in some) [OMIM:Cirrhosis (in some)]
Cirrhosis (rare) [OMIM:Cirrhosis (rare)]
Compensated cirrhosis [OMIM:Compensated cirrhosis]
Quality:
Cross references:
Orphanet:29120 "Cirrhosis" [Orphanet:29120]
OMIM: "Cirrhosis" [OMIM:Cirrhosis]
OMIM: "Hepatic cirrhosis" [OMIM:Hepatic cirrhosis]
OMIM: "Liver cirrhosis" [OMIM:Liver cirrhosis]
OMIM: "Cirrhosis (1 patient)" [OMIM:Cirrhosis (1 patient)]
OMIM: "Cirrhosis (in late-onset cases)" [OMIM:Cirrhosis (in late-onset cases)]
OMIM: "Cirrhosis (in some patients)" [OMIM:Cirrhosis (in some patients)]
OMIM: "Cirrhosis (in some)" [OMIM:Cirrhosis (in some)]
OMIM: "Cirrhosis (rare)" [OMIM:Cirrhosis (rare)]
OMIM: "Compensated cirrhosis" [OMIM:Compensated cirrhosis]
UMLS:C0023890 "Cirrhosis" [HPO:0001394]
UMLS:C0023890 "Liver Cirrhosis" [Orphanet:29120]
UMLS:C1623038 "Cirrhosis" [Orphanet:29120]
Is a (Direct Parents):
HPO         Abnormality of the liver
Orphanet Decreased liver function
MedDRA Hepatic fibrosis and 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)
MedDRA:
Hepatobiliary disorders(MedDRA:10019805)
    Hepatic and hepatobiliary disorders(MedDRA:10019654)
       Hepatic fibrosis and cirrhosis(MedDRA:10019669)
          Cirrhosis(HPO:0001394)
Database Frequency: 102 / 7739
Resource:

All diseases associated with this symptom:

Aarskog-Scott syndrome (Orphanet:915)
Acute interstitial pneumonia (Orphanet:79126)
Adams-Oliver syndrome (Orphanet:974)
Alagille syndrome due to 20p12 microdeletion (Orphanet:261600)
Alagille syndrome due to a JAG1 point mutation (Orphanet:261619)
Alpers syndrome (Orphanet:726)
Alpha-1-antitrypsin deficiency (Orphanet:60)
Alström syndrome (Orphanet:64)
Alveolar echinococcosis (Orphanet:284)
Argininemia (Orphanet:90)
Argininosuccinic aciduria (Orphanet:23)
Arthrogryposis - renal dysfunction - cholestasis (Orphanet:2697)
Autoimmune polyendocrinopathy type 2 (Orphanet:3143)
BERRY ANEURYSM, CIRRHOSIS, PULMONARY EMPHYSEMA, AND CEREBRAL CALCIFICATION (OMIM:210050)
Benign recurrent intrahepatic cholestasis (Orphanet:65682)
Berardinelli-Seip congenital lipodystrophy (Orphanet:528)
Beta-thalassemia major (Orphanet:231214)
Biliary atresia (Orphanet:30391)
Budd-Chiari syndrome (Orphanet:131)
CIRRHOSIS, FAMILIAL (OMIM:118900)
COG4-CDG (Orphanet:263501)
Cholestasis - lymphedema (Orphanet:1414)
Cholesteryl ester storage disease (Orphanet:75234)
Cirrhosis-dystonia-polycythemia-hypermanganesemia syndrome (Orphanet:309854)
Cirrhotic cardiomyopathy (Orphanet:57777)
Citrullinemia type I (Orphanet:247525)
Classic galactosemia (Orphanet:79239)
Congenital bile acid synthesis defect type 1 (Orphanet:79301)
Congenital bile acid synthesis defect type 2 (Orphanet:79303)
Congenital bile acid synthesis defect type 3 (Orphanet:79302)
Congenital bile acid synthesis defect type 4 (Orphanet:79095)
Cranioectodermal dysplasia 3 (OMIM:614099)
Cryptosporidiosis - chronic cholangitis - liver disease (Orphanet:357329)
DYSKERATOSIS CONGENITA, AUTOSOMAL DOMINANT, 1 (OMIM:127550)
DYSKERATOSIS CONGENITA, AUTOSOMAL RECESSIVE, 2 (OMIM:613987)
Distomatosis (Orphanet:1685)
Dyskeratosis congenita (Orphanet:1775)
Erythropoietic protoporphyria (Orphanet:79278)
Familial partial lipodystrophy associated with PPARG mutations (Orphanet:79083)
GLYCOGEN STORAGE DISEASE IXc (OMIM:613027)
GRACILE syndrome (Orphanet:53693)
Gaucher disease (Orphanet:355)
Gaucher disease type 1 (Orphanet:77259)
Gaucher disease type 2 (Orphanet:77260)
Gaucher disease type 3 (Orphanet:77261)
Glycogen storage disease due to glycogen branching enzyme deficiency (Orphanet:367)
Glycogen storage disease due to glycogen branching enzyme deficiency, adult neuromuscular form (Orphanet:308712)
Glycogen storage disease due to glycogen branching enzyme deficiency, childhood combined hepatic and myopathic form (Orphanet:308684)
Glycogen storage disease due to glycogen branching enzyme deficiency, childhood neuromuscular form (Orphanet:308698)
Glycogen storage disease due to glycogen branching enzyme deficiency, congenital neuromuscular form (Orphanet:308670)
Glycogen storage disease due to glycogen branching enzyme deficiency, fatal perinatal neuromuscular form (Orphanet:308655)
Glycogen storage disease due to glycogen branching enzyme deficiency, non progressive hepatic form (Orphanet:308638)
Glycogen storage disease due to glycogen branching enzyme deficiency, progressive hepatic form (Orphanet:308621)
Hemochromatosis type 2 (Orphanet:79230)
Hemochromatosis type 3 (Orphanet:225123)
Hemochromatosis type 4 (Orphanet:139491)
Hemochromatosis, type 1 (OMIM:235200)
Hemochromatosis, type 2A (OMIM:602390)
Hemochromatosis, type 2B (OMIM:613313)
Hepatoencephalopathy due to combined oxidative phosphorylation deficiency type 1 (Orphanet:137681)
Hepatoerythropoietic porphyria (Orphanet:95159)
Hereditary fructose intolerance (Orphanet:469)
Hereditary hemorrhagic telangiectasia (Orphanet:774)
Hoyeraal-Hreidarsson syndrome (Orphanet:3322)
Hydatidosis (Orphanet:400)
ICHTHYOSIFORM ERYTHRODERMA, CORNEAL INVOLVEMENT, AND DEAFNESS (OMIM:242150)
INFANTILE LIVER FAILURE SYNDROME 2 (OMIM:615486)
Idiopathic pulmonary fibrosis (Orphanet:2032)
Joubert syndrome with hepatic defect (Orphanet:1454)
LIPODYSTROPHY, CONGENITAL GENERALIZED, TYPE 1 (OMIM:608594)
LIPODYSTROPHY, CONGENITAL GENERALIZED, TYPE 2 (OMIM:269700)
Long chain 3-hydroxyacyl-CoA dehydrogenase deficiency (Orphanet:5)
MEDNIK syndrome (Orphanet:171851)
MPI-CDG (Orphanet:79319)
Mulibrey nanism (Orphanet:2576)
Multiple congenital anomalies-hypotonia-seizures syndrome type 2 (Orphanet:300496)
Navajo neurohepatopathy (Orphanet:255229)
Neonatal hemochromatosis (Orphanet:446)
Neonatal intrahepatic cholestasis due to citrin deficiency (Orphanet:247598)
PULMONARY FIBROSIS AND/OR BONE MARROW FAILURE, TELOMERE-RELATED, 1 (OMIM:614742)
PULMONARY FIBROSIS AND/OR BONE MARROW FAILURE, TELOMERE-RELATED, 2 (OMIM:614743)
Porphyria cutanea tarda (Orphanet:101330)
Primary lipodystrophy (Orphanet:90970)
Progressive familial intrahepatic cholestasis (Orphanet:172)
Progressive familial intrahepatic cholestasis type 1 (Orphanet:79306)
Progressive familial intrahepatic cholestasis type 2 (Orphanet:79304)
Progressive familial intrahepatic cholestasis type 3 (Orphanet:79305)
RENAL-HEPATIC-PANCREATIC DYSPLASIA 1 (OMIM:208540)
Renal-hepatic-pancreatic dysplasia (Orphanet:294415)
Reynolds syndrome (Orphanet:779)
SPLENOPORTAL VASCULAR ANOMALIES (OMIM:271500)
Scleroderma (Orphanet:801)
Sea-blue histiocytosis (Orphanet:158029)
Syndromic diarrhea (Orphanet:84064)
Systemic mastocytosis (Orphanet:2467)
TELANGIECTASIA, HEREDITARY HEMORRHAGIC, OF RENDU, OSLER, AND WEBER (OMIM:187300)
TELANGIECTASIA, HEREDITARY HEMORRHAGIC, TYPE 2 (OMIM:600376)
TRICHOHEPATOENTERIC SYNDROME 1 (OMIM:222470)
TRICHOHEPATOENTERIC SYNDROME 2 (OMIM:614602)
Transaldolase deficiency (Orphanet:101028)
Tyrosinemia type 1 (Orphanet:882)
Wilson disease (Orphanet:905)