Acute liver failure




Input patient's signs and symptoms


Narrow down the case reports



Total: 1411 (papers)

  


(per page)
Matched Phenotype  Gene  Mutation  MeSH
Rank
(Similarity)
PMID
(PMCID)
1
(59.7%)
12394969
Sickle cell disease, extreme hyperbilirubinemia, and pericardial tamponade: case report and review of the literature.
Khurshid I, Anderson L, Downie GH, Pape GS.
Crit Care Med. 2002;30(10):2363-7.
Intrahepatic cholestasis Anemia Hepatomegaly Hyperbilirubinemia
Adult Anemia, Sickle Cell Cardiac Tamponade Exchange Transfusion, Whole Blood Homo sapiens Hyperbilirubinemia Intrahepatic Cholestasis Liver Failure Male
2
(57.4%)
26397283
[Hemophagocytic lymphohistiocytosis presenting as acute liver failure in a patient with Hodgkin lymphoma: case report and review of the literature].
Bravo-Jaimes KM.
Rev Gastroenterol Peru. 2015;35(3):256-7.
Jaundice Anemia Fever Lymphadenopathy
Females Hodgkin Disease Homo sapiens Liver Failure, Acute Lymphohistiocytosis, Hemophagocytic
3
(56.4%)
12217711
Fulminant hepatic failure and autoimmune hemolytic anemia associated with Epstein-Barr virus infection.
Palanduz A, Yildirmak Y, Telhan L, Arapoglu M, Urganci N, Tufekci S, Kayaalp N.
J Infect. 2002;45(2):96-8.
Jaundice Splenomegaly Anemia
Adrenal Cortex Hormones Anti-Bacterial Agents Antifibrinolytic Agents Blood Transfusion Child Epstein-Barr Virus Infections Females Gastrointestinal Agents Homo sapiens Liver Failure Plasma
4
(56.2%)
11827656
[Difficulties in the diagnosis of familial hemophagocytic lymphohistiocytosis].
Astigarraga Aguirre I, Navajas Gutierrez A, Fernandez-Teijeiro Alvarez A, Latorre Garcia J, Aldamiz-Echevarria Azuara L.
An Esp Pediatr. 2002;56(2):168-70.
Splenomegaly Anemia Fever
Fatal Outcome Females Histiocytosis, Non-Langerhans-Cell Homo sapiens Infant
5
(55.1%)
30922274
EIF2AK3 novel mutation in a child with early-onset diabetes mellitus, a case report.
Fatani TH.
BMC Pediatr. 2019;19(1):85.
Diabetes mellitus Microcytic anemia Hepatomegaly
EIF2AK3
Child, Preschool Diabetes Mellitus, Insulin-Dependent Fatal Outcome Females Homo sapiens Infant, Newborn Neonatal Screening Osteochondrodysplasias Septic Shock eIF-2 Kinase
5
(55.1%)
19203989
Parvovirus B19-induced thrombocytopenia and anemia in a child with fatal fulminant hepatic failure coinfected with hepatitis A and E viruses.
Kishore J, Sen M.
J Trop Pediatr. 2009;55(5):335-7.
Hepatosplenomegaly Reticulocytopenia Anemia Fever
Anemia Child, Preschool Fatal Outcome Hepatitis A Hepatitis E Homo sapiens Liver Failure, Acute Male Polymerase Chain Reaction Thrombocytopenia
7
(54.4%)
28858213
(5618200)
Recreational Exposure during Algal Bloom in Carrasco Beach, Uruguay: A Liver Failure Case Report.
Vidal F, Sedan D, D'Agostino D, Cavalieri ML, Mullen E, Parot Varela MM, Flores C, Caixach J, Andrinolo D.
Toxins (Basel). 2017;9(9):.
Jaundice Anemia Hepatomegaly
Alanine Transaminase Aspartate Transaminase Bathing Beaches Bilirubin Environmental Exposure Females Harmful Algal Bloom Homo sapiens Infant Liver Liver Failure Microcystins Uruguay Water Pollutants
8
(54.2%)
27893685
(5134878)
Acute liver failure caused by hemophagocytic lymphohistiocytosis in adults: A case report and review of the literature.
Lin S, Li Y, Long J, Liu Q, Yang F, He Y.
Medicine (Baltimore). 2016;95(47):e5431.
Jaundice Anemia Hypertriglyceridemia
Adult Biopsy Fatal Outcome Homo sapiens Liver Failure, Acute Lymphohistiocytosis, Hemophagocytic Male
9
(51.4%)
26465220
Hepatic Compartment Syndrome Following Percutaneous Cholecystostomy: A Case Report.
Marcaire F, Malavieille F, Pichot-Delahaye V, Floccard B, Rimmele T.
Crit Care Med. 2016;44(3):e174-7.
Cholecystitis Anemia Metabolic acidosis
Budd-Chiari Syndrome Cholecystostomy Fatal Outcome Gastric Bypass Hematoma Homo sapiens Intra-Abdominal Hypertension Liver Male Middle Aged Postoperative Complications Ultrasonography
10
(49.7%)
24991218
(4065746)
Rare Manifestation of a Rare Disease, Acute Liver Failure in Adult Onset Still's Disease: Dramatic Response to Methylprednisolone Pulse Therapy-A Case Report and Review.
Valluru N, Tammana VS, Windham M, Mekonen E, Begum R, Sanderson A.
Case Rep Med. 2014;2014:375035.
Jaundice Fever Leukocytosis Hepatomegaly
        

Phenotype(s) retrieved from Orphanet

    Total: 0

HPO ID Term Frequency


Phenotype(s) retrieved from case reports

    Total: 200

HPO ID Term # of case reports
HP:0012115 Hepatitis 143
HP:0001298 Encephalopathy 50
HP:0001394 Cirrhosis 43
HP:0002480 Hepatic encephalopathy 38
HP:0200119 Acute hepatitis 38
HP:0001945 Fever 29
HP:0000952 Jaundice 26
HP:0006562 Viral hepatitis 21
HP:0031273 Shock 20
HP:0002181 Cerebral edema 17
HP:0200123 Chronic hepatitis 17
HP:0001919 Acute kidney injury 13
HP:0002605 Hepatic necrosis 13
HP:0003201 Rhabdomyolysis 13
HP:0001297 Stroke 12
HP:0001396 Cholestasis 12
HP:0001878 Hemolytic anemia 12
HP:0005521 Disseminated intravascular coagulation 12
HP:0100806 Sepsis 12
HP:0001250 Seizures 10
HP:0001541 Ascites 10
HP:0001873 Thrombocytopenia 10
HP:0001876 Pancytopenia 10
HP:0002098 Respiratory distress 10
HP:0004787 Fulminant hepatitis 10
HP:0030731 Carcinoma 10
HP:0001399 Hepatic failure 9
HP:0001733 Pancreatitis 9
HP:0000822 Hypertension 8
HP:0001635 Congestive heart failure 8
HP:0001903 Anemia 8
HP:0001909 Leukemia 8
HP:0002240 Hepatomegaly 8
HP:0002721 Immunodeficiency 8
HP:0002861 Melanoma 8
HP:0002904 Hyperbilirubinemia 8
HP:0001406 Intrahepatic cholestasis 7
HP:0001735 Acute pancreatitis 7
HP:0003128 Lactic acidosis 7
HP:0000836 Hyperthyroidism 6
HP:0002027 Abdominal pain 6
HP:0002878 Respiratory failure 6
HP:0000969 Edema 5
HP:0001987 Hyperammonemia 5
HP:0030357 Small cell lung carcinoma 5
HP:0000083 Renal insufficiency 4
HP:0000988 Skin rash 4
HP:0001409 Portal hypertension 4
HP:0001638 Cardiomyopathy 4
HP:0001824 Weight loss 4
HP:0001943 Hypoglycemia 4
HP:0002013 Vomiting 4
HP:0002039 Anorexia 4
HP:0002315 Headache 4
HP:0002615 Hypotension 4
HP:0100279 Ulcerative colitis 4
HP:0000100 Nephrotic syndrome 3
HP:0001082 Cholecystitis 3
HP:0001404 Hepatocellular necrosis 3
HP:0001658 Myocardial infarction 3
HP:0001942 Metabolic acidosis 3
HP:0002045 Hypothermia 3
HP:0002090 Pneumonia 3
HP:0002204 Pulmonary embolism 3
HP:0002647 Aortic dissection 3
HP:0002716 Lymphadenopathy 3
HP:0002719 Recurrent infections 3
HP:0003002 Breast carcinoma 3
HP:0003073 Hypoalbuminemia 3
HP:0005912 Biliary atresia 3
HP:0012125 Prostate cancer 3
HP:0012156 Hemophagocytosis 3
HP:0030149 Cardiogenic shock 3
HP:0030151 Cholangitis 3
HP:0100519 Anuria 3
HP:0200084 Giant cell hepatitis 3
HP:0000846 Adrenal insufficiency 2
HP:0001251 Ataxia 2
HP:0001287 Meningitis 2
HP:0001289 Confusion 2
HP:0001433 Hepatosplenomegaly 2
HP:0001744 Splenomegaly 2
HP:0001880 Eosinophilia 2
HP:0001994 Renal Fanconi syndrome 2
HP:0002014 Diarrhea 2
HP:0002018 Nausea 2
HP:0002133 Status epilepticus 2
HP:0002148 Hypophosphatemia 2
HP:0002448 Progressive encephalopathy 2
HP:0002516 Increased intracranial pressure 2
HP:0002583 Colitis 2
HP:0002613 Biliary cirrhosis 2
HP:0002652 Skeletal dysplasia 2
HP:0004900 Severe lactic acidosis 2
HP:0004947 Arteriovenous fistula 2
HP:0005110 Atrial fibrillation 2
HP:0008682 Acute tubular necrosis 2
HP:0011675 Arrhythmia 2
HP:0012819 Myocarditis 2
HP:0020071 Viremia 2
HP:0025615 Abscess 2
HP:0030243 Hepatic vein thrombosis 2
HP:0030955 Alcoholism 2
HP:0031864 Bacteremia 2
HP:0032368 Acidemia 2
HP:0100598 Pulmonary edema 2
HP:0200032 Kayser-Fleischer ring 2
HP:0000071 Ureteral stenosis 1
HP:0000099 Glomerulonephritis 1
HP:0000112 Nephropathy 1
HP:0000123 Nephritis 1
HP:0000421 Epistaxis 1
HP:0000520 Proptosis 1
HP:0000572 Visual loss 1
HP:0000618 Blindness 1
HP:0000651 Diplopia 1
HP:0000709 Psychosis 1
HP:0000789 Infertility 1
HP:0000821 Hypothyroidism 1
HP:0000842 Hyperinsulinemia 1
HP:0000989 Pruritus 1
HP:0001258 Spastic paraplegia 1
HP:0001260 Dysarthria 1
HP:0001300 Parkinsonism 1
HP:0001332 Dystonia 1
HP:0001337 Tremor 1
HP:0001369 Arthritis 1
HP:0001370 Rheumatoid arthritis 1
HP:0001395 Hepatic fibrosis 1
HP:0001508 Failure to thrive 1
HP:0001513 Obesity 1
HP:0001537 Umbilical hernia 1
HP:0001678 Atrioventricular block 1
HP:0001698 Pericardial effusion 1
HP:0001701 Pericarditis 1
HP:0001875 Neutropenia 1
HP:0001907 Thromboembolism 1
HP:0001941 Acidosis 1
HP:0002017 Nausea and vomiting 1
HP:0002040 Esophageal varix 1
HP:0002047 Malignant hyperthermia 1
HP:0002093 Respiratory insufficiency 1
HP:0002097 Emphysema 1
HP:0002149 Hyperuricemia 1
HP:0002170 Intracranial hemorrhage 1
HP:0002248 Hematemesis 1
HP:0002352 Leukoencephalopathy 1
HP:0002488 Acute leukemia 1
HP:0002584 Intestinal bleeding 1
HP:0002586 Peritonitis 1
HP:0002612 Congenital hepatic fibrosis 1
HP:0002619 Varicose veins 1
HP:0002656 Epiphyseal dysplasia 1
HP:0002664 Neoplasm 1
HP:0002748 Rickets 1
HP:0002902 Hyponatremia 1
HP:0003003 Colon cancer 1
HP:0003124 Hypercholesterolemia 1
HP:0003198 Myopathy 1
HP:0003326 Myalgia 1
HP:0004322 Short stature 1
HP:0004420 Arterial thrombosis 1
HP:0004749 Atrial flutter 1
HP:0004756 Ventricular tachycardia 1
HP:0004933 Ascending aortic dissection 1
HP:0004936 Venous thrombosis 1
HP:0005263 Gastritis 1
HP:0005523 Lymphoproliferative disorder 1
HP:0005575 Hemolytic-uremic syndrome 1
HP:0006740 Transitional cell carcinoma of the bladder 1
HP:0008281 Acute hyperammonemia 1
HP:0008940 Generalized lymphadenopathy 1
HP:0008942 Acute rhabdomyolysis 1
HP:0010783 Erythema 1
HP:0011110 Tonsillitis 1
HP:0011896 Subconjunctival hemorrhage 1
HP:0012133 Erythroid hypoplasia 1
HP:0012175 Resistance to activated protein C 1
HP:0012223 Splenic rupture 1
HP:0012251 ST segment elevation 1
HP:0012330 Pyelonephritis 1
HP:0012444 Brain atrophy 1
HP:0012532 Chronic pain 1
HP:0012578 Membranous nephropathy 1
HP:0030049 Brain abscess 1
HP:0030127 Endometriosis 1
HP:0030242 Portal vein thrombosis 1
HP:0031035 Chronic infection 1
HP:0032199 Abnormal prothrombin time 1
HP:0032252 Granuloma 1
HP:0040223 Pulmonary hemorrhage 1
HP:0100309 Subdural hemorrhage 1
HP:0100523 Liver abscess 1
HP:0100584 Endocarditis 1
HP:0100601 Eclampsia 1
HP:0100758 Gangrene 1
HP:0100762 Hemobilia 1
HP:0100768 Choriocarcinoma 1
HP:0200120 Chronic active hepatitis 1
HP:0410281 Dyspepsia 1


Causative gene(s) retrieved from Orphanet

    Total: 0

Gene Symbol Gene Name Entrez Gene ID