Cirrhosis
Symptom Information:
Symptom ID: | HPO:0001394 | |||||||||||||||||||||||||||
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) MedDRA: Hepatobiliary disorders(MedDRA:10019805) Hepatic and hepatobiliary disorders(MedDRA:10019654) Hepatic fibrosis and cirrhosis(MedDRA:10019669) Cirrhosis(HPO:0001394) |
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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) |