Hepatic failure

Symptom Information:

Symptom ID: HPO:0001399
Synonyms:
Liver failure [HPO:0001399]
Hepatic failure (disorder) [Orphanet:29240]
Liver Failure [Orphanet:29240]
Hepatic failure [OMIM:Hepatic failure]
Liver failure [OMIM:Liver failure]
Hepatocellular liver disease/hepatic failure [Orphanet:29240]
Hepatic failure [Orphanet:29240]
Hepatic failure [MedDRA:10019663]
Failure liver [MedDRA:10019663]
Liver failure [MedDRA:10019663]
Hepatic insufficiency [MedDRA:10019663]
Hepatobiliary insufficiency [MedDRA:10019663]
Hepatic failure (less common) [OMIM:Hepatic failure (less common)]
Hepatic failure (reported in 1 patient) [OMIM:Hepatic failure (reported in 1 patient)]
Liver failure (1 patient) [OMIM:Liver failure (1 patient)]
Liver failure (in some patients) [OMIM:Liver failure (in some patients)]
Quality:
Cross references:
Orphanet:29240 "Hepatocellular liver disease/hepatic failure" [Orphanet:29240]
OMIM: "Hepatic failure" [OMIM:Hepatic failure]
OMIM: "Liver failure" [OMIM:Liver failure]
OMIM: "Hepatic failure (less common)" [OMIM:Hepatic failure (less common)]
OMIM: "Hepatic failure (reported in 1 patient)" [OMIM:Hepatic failure (reported in 1 patient)]
OMIM: "Liver failure (1 patient)" [OMIM:Liver failure (1 patient)]
OMIM: "Liver failure (in some patients)" [OMIM:Liver failure (in some patients)]
UMLS:C0085605 "Liver Failure" [Orphanet:29240]
Is a (Direct Parents):
MedDRA Hepatic failure and associated disorders
Orphanet Decreased liver function
HPO         Decreased liver function
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)
                Decreased liver function(HPO:0001410)
                   Hepatic failure(HPO:0001399)
MedDRA:
Hepatobiliary disorders(MedDRA:10019805)
    Hepatic and hepatobiliary disorders(MedDRA:10019654)
       Hepatic failure and associated disorders(MedDRA:10019664)
          Hepatic failure(HPO:0001399)
Database Frequency: 80 / 7739
Resource:

All diseases associated with this symptom:

ALG1-CDG (Orphanet:79327)
ALG6-CDG (Orphanet:79320)
ALG8-CDG (Orphanet:79325)
ALG9-CDG (Orphanet:79328)
Acyl-CoA dehydrogenase 9 deficiency (Orphanet:99901)
Alpers syndrome (Orphanet:726)
Alpha-1-antitrypsin deficiency (Orphanet:60)
Alström syndrome (Orphanet:64)
Aromatase deficiency (Orphanet:91)
BERRY ANEURYSM, CIRRHOSIS, PULMONARY EMPHYSEMA, AND CEREBRAL CALCIFICATION (OMIM:210050)
BILE ACID SYNTHESIS DEFECT, CONGENITAL, 5 (OMIM:616278)
Babesiosis (Orphanet:108)
Bardet-Biedl syndrome (Orphanet:110)
Berardinelli-Seip congenital lipodystrophy (Orphanet:528)
Budd-Chiari syndrome (Orphanet:131)
CEROID STORAGE DISEASE (OMIM:214200)
CHOLESTASIS, PROGRESSIVE FAMILIAL INTRAHEPATIC, 4 (OMIM:615878)
COENZYME Q10 DEFICIENCY, PRIMARY, 1 (OMIM:607426)
COG4-CDG (Orphanet:263501)
Carnitine palmitoyl transferase 1A deficiency (Orphanet:156)
Carnitine palmitoyl transferase II deficiency, severe infantile form (Orphanet:228305)
Cholesteryl ester storage disease (Orphanet:75234)
Cirrhotic cardiomyopathy (Orphanet:57777)
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 (Orphanet:1515)
Cranioectodermal dysplasia 1 (OMIM:218330)
Cryoglobulinemic vasculitis (Orphanet:91138)
Cryptosporidiosis - chronic cholangitis - liver disease (Orphanet:357329)
Dyskeratosis congenita (Orphanet:1775)
Erythropoietic protoporphyria (Orphanet:79278)
Fatal mitochondrial disease due to combined oxidative phosphorylation deficiency 3 (Orphanet:168566)
Fetal Gaucher disease (Orphanet:85212)
Fumaric aciduria (Orphanet:24)
GCS1-CDG (Orphanet:79330)
Galactosemia (Orphanet:352)
Gaucher disease type 2 (Orphanet:77260)
Giant cell arteritis (Orphanet:397)
Glycogen storage disease due to glycogen branching enzyme deficiency (Orphanet:367)
Glycogen storage disease due to glycogen branching enzyme deficiency, progressive hepatic form (Orphanet:308621)
Hashimoto-Pritzker syndrome (Orphanet:99872)
Hepatoencephalopathy due to combined oxidative phosphorylation deficiency type 1 (Orphanet:137681)
Hereditary hemorrhagic telangiectasia (Orphanet:774)
Hyperammonemia due to N-acetylglutamate synthetase deficiency (Orphanet:927)
Infantile neuronal ceroid lipofuscinosis (Orphanet:79263)
Isolated NADH-CoQ reductase deficiency (Orphanet:2609)
Johanson-Blizzard syndrome (Orphanet:2315)
LYMPHOPROLIFERATIVE SYNDROME, X-LINKED, 1 (OMIM:308240)
Lafora disease (Orphanet:501)
Lathosterolosis (Orphanet:46059)
Leigh syndrome (Orphanet:506)
Lujo hemorrhagic fever (Orphanet:319213)
MERRF (Orphanet:551)
MPI-CDG (Orphanet:79319)
Mitochondrial DNA depletion syndrome, hepatocerebral form due to DGUOK deficiency (Orphanet:279934)
Mullerian derivatives - lymphangiectasia - polydactyly (Orphanet:1655)
Navajo neurohepatopathy (Orphanet:255229)
Neonatal hemochromatosis (Orphanet:446)
Neonatal intrahepatic cholestasis due to citrin deficiency (Orphanet:247598)
Nephronophthisis 15 (OMIM:614845)
Nodular regenerative hyperplasia of the liver (Orphanet:48372)
Odontomatosis - aortae esophagus stenosis (Orphanet:2724)
Ornithine transcarbamylase deficiency (Orphanet:664)
PROTOPORPHYRIA, ERYTHROPOIETIC (OMIM:177000)
Phosphoenolpyruvate carboxykinase 1 deficiency (Orphanet:79316)
Phosphoenolpyruvate carboxykinase 2 deficiency (Orphanet:79317)
Phosphoenolpyruvate carboxykinase deficiency (Orphanet:2880)
Pyruvate dehydrogenase E3 deficiency (Orphanet:2394)
Rift valley fever (Orphanet:319251)
Short-rib thoracic dysplasia 10 with or without polydactyly (OMIM:615630)
Steroid dehydrogenase deficiency - dental anomalies (Orphanet:3196)
Syndromic diarrhea (Orphanet:84064)
Transaldolase deficiency (Orphanet:101028)
Very long chain acyl-CoA dehydrogenase deficiency (Orphanet:26793)
Wilson disease (Orphanet:905)
Wolman disease (Orphanet:75233)
Zellweger syndrome (Orphanet:912)