Hepatic failure
Symptom Information:
Symptom ID: | HPO:0001399 | ||||||||||||||||
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) 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) |
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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) |