Informaţii despre

Nume Liver Disease
Pagina Web www.malacards.org
Clasificare globală Malacards Boli genetice; Boli metabolice; Boli rare
Clasificari ICD10 Hepatic failure, unspecified; Liver disease, unspecified; Liver disorders in other diseases classified elsewhere; Other specified diseases of liver
Clasificare anatomică Malacards Boli gastrointestinale; Boli hepatice
Boli din aceeaşi familie Acute Liver Failure; Infantile Liver Failure Syndrome 1; Infantile Liver Failure Syndrome 2; Liver Failure, Infantile, Transient

Vezi şi

Boli A-Z 3-Hydroxyacyl-Coa Dehydrogenase Deficiency Abdominal Obesity-Metabolic Syndrome 1 Acanthosis Nigricans Acquired Generalized Lipodystrophy Acquired Immunodeficiency Syndrome Acquired Metabolic Disease Acrocallosal Syndrome Acute Liver Failure Adenocarcinoma Adenoma Adenosine Deaminase Deficiency Adrenal Adenoma Adult Polyglucosan Body Disease Adult Respiratory Distress Syndrome Aging Alagille Syndrome 1 Al Amyloidosis Aland Island Eye Disease Albinism-Deafness Syndrome Alcohol Abuse Alcohol Dependence Alcoholic Cardiomyopathy Alcoholic Hepatitis Alcoholic Liver Cirrhosis Alcoholic Pancreatitis Alkaline Phosphatase, Plasma Level of, Quantitative Trait Locus 1 Alopecia, Neurologic Defects, and Endocrinopathy Syndrome Alpha-1-Antitrypsin Deficiency Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity Alpha-Fetoprotein Deficiency Alport Syndrome, X-Linked Al-Raqad Syndrome Alstrom Syndrome Alzheimer Disease 3 Amyloid Neuropathy Amyloidosis Amyloidosis Beta2m Analbuminemia Anauxetic Dysplasia 1 Ancylostomiasis Aneurysm Angiosarcoma Aniridia 1 Anorexia Nervosa 1 Antipyrine Metabolism Apnea, Obstructive Sleep Arteries, Anomalies of Arteriosclerosis Obliterans Arteriovenous Fistula Arthritis Arthrochalasia Ehlers-Danlos Syndrome Aspergillosis Astrocytoma Ataxia and Polyneuropathy, Adult-Onset Ataxia-Telangiectasia Atp8b1 Deficiency Atransferrinemia Atrial Fibrillation Australia Antigen Autoimmune Disease of Urogenital Tract Autoimmune Hepatitis Autoinflammation, Lipodystrophy, and Dermatosis Syndrome Autonomic Dysfunction Autosomal Dominant Polycystic Kidney Disease Banti's Syndrome B-Cell Lymphomas Beta-Adrenergic Stimulation, Response to Beta-Thalassemia Bile Duct Carcinoma Bile Duct Disease Biliary Atresia Biliary Tract Disease Bilirubin Metabolic Disorder Bipolar Disorder Bleeding Disorder, Platelet-Type, 11 Blood Group--Ahonen Blood Group, Dombrock System Blood Group, I System Body Mass Index Quantitative Trait Locus 10 Body Mass Index Quantitative Trait Locus 11 Body Mass Index Quantitative Trait Locus 12 Body Mass Index Quantitative Trait Locus 14 Body Mass Index Quantitative Trait Locus 18 Body Mass Index Quantitative Trait Locus 4 Body Mass Index Quantitative Trait Locus 7 Body Mass Index Quantitative Trait Locus 8 Body Mass Index Quantitative Trait Locus 9 Bone Fracture Bone Mineral Density Quantitative Trait Locus 15 Bone Mineral Density Quantitative Trait Locus 8 Bornholm Eye Disease Brain Cancer Brain Edema Breast Cancer Brucellosis Budd-Chiari Syndrome Bullous Lichen Planus Burns Calciphylaxis Candidiasis Cardiac Arrest Carotid Artery Dissection Cataract 5, Multiple Types Celiac Disease 1 Central Nervous System Disease Cerebellar Astrocytoma Cerebral Aneurysms Cerebral Atrophy Cerebral Degeneration Cerebritis Cerebrotendinous Xanthomatosis Cholangiocarcinoma Cholangitis Cholangitis, Primary Sclerosing Cholecystitis Cholecystolithiasis Choledocholithiasis Cholelithiasis Cholestasis Cholestasis, Benign Recurrent Intrahepatic, 1 Cholestasis-Lymphedema Syndrome Cholestasis, Progressive Familial Intrahepatic, 1 Cholestasis, Progressive Familial Intrahepatic, 2 Cholestasis, Progressive Familial Intrahepatic, 3 Choline Deficiency Disease Chronic Enteropathy Associated with Slco2a1 Gene Chronic Myelomonocytic Leukemia Chronic Pulmonary Heart Disease Cirrhotic Cardiomyopathy Citrullinemia, Type Ii, Neonatal-Onset Cleft Larynx, Posterior Cleft Palate, Isolated Coccidioidomycosis Cohen-Gibson Syndrome Colitis Collagen Disease Colorectal Adenoma Colorectal Cancer Common Variable Immunodeficiency Compartment Syndrome Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy Cone Dystrophy Congenital Hepatic Fibrosis Congestive Heart Failure Conjunctivitis Connective Tissue Disease Constrictive Pericarditis Crimean-Congo Hemorrhagic Fever Critical Limb Ischemia Cryoglobulinemia Cryptococcosis Cryptogenic Cirrhosis Cryptosporidiosis Cystadenocarcinoma Cystathioninuria Cystic Angiomatosis of Bone, Diffuse Cystic Fibrosis Cystinosis Cytomegalovirus Infection Dengue Hemorrhagic Fever Dermatitis Diabetes Mellitus Diarrhea Digeorge Syndrome Disseminated Intravascular Coagulation Down Syndrome Dubin-Johnson Syndrome Duodenal Ulcer Duodenitis Dysautonomia Dysfibrinogenemia Dyskeratosis Congenita Dystonia Dystonia/parkinsonism, Hypermanganesemia, Polycythemia, and Chronic Liver Disease Eales Disease Eclampsia Encephalopathy Endocarditis Endodermal Sinus Tumor Endotheliitis End Stage Renal Failure Epileptic Encephalopathy, Early Infantile, 36 Epiphyseal Dysplasia, Multiple, with Early-Onset Diabetes Mellitus Epithelial Recurrent Erosion Dystrophy Epstein-Barr Virus Hepatitis Esophageal Candidiasis Esophageal Varix Exfoliative Dermatitis Exocrine Pancreatic Insufficiency Extrahepatic Cholestasis Familial Mediterranean Fever Fanconi Anemia, Complementation Group E Fanconi Renotubular Syndrome 1 Fanconi Syndrome Fasciitis Fascioliasis Fatty Liver Disease Fibromatosis, Gingival, 1 Food Allergy Fournier Gangrene Friedreich Ataxia 1 Fundus Albipunctatus Fungal Esophagitis Galactosemia Gallbladder Disease Gastric Antral Vascular Ectasia Gastric Cancer Gastroenteritis Gastroesophageal Reflux Gastrointestinal System Disease Gastroschisis Genitopatellar Syndrome Gerstmann-Straussler Disease Giant Hemangioma Giardioză Gilles De La Tourette Syndrome Glaucoma-Related Pigment Dispersion Syndrome Glomerulonephritis Glucagonoma Glucose Intolerance Glucose Metabolism Disease Glycogen Storage Disease Growth Control, Y-Chromosome Influenced Guillain-Barre Syndrome, Familial Hairy Cell Leukemia Halothane Hepatitis Helicobacter Pylori Infection Hellp Syndrome Hemochromatosis, Neonatal Hemochromatosis, Type 1 Hemolytic Anemia Hemophagocytic Lymphohistiocytosis Hemophilia Hemophilia a Hemorrhagic Disease Hemorrhagic Fever Hemosiderosis Hepadnavirus Infection Heparin-Induced Thrombocytopenia Hepatic Adenomas, Familial Hepatic Coma Hepatic Encephalopathy Hepatic Tuberculosis Hepatic Vascular Disease Hepatic Veno-Occlusive Disease Hepatitis Hepatitis a Hepatitis B Hepatitis C Hepatitis C Virus Hepatitis D Hepatitis E Hepatocellular Adenoma Hepatocellular Carcinoma Hepatoportal Sclerosis Hepatopulmonary Syndrome Hepatorenal Syndrome Hereditary Hemorrhagic Telangiectasia Histiocytosis Human Coronavirus Sensitivity Hydrolethalus Syndrome 1 Hydrops, Lactic Acidosis, and Sideroblastic Anemia Hyperandrogenism Hypercholesterolemia, Autosomal Dominant, 3 Hypereosinophilic Syndrome Hyperferritinemia with or Without Cataract Hyperglycemia Hyperphosphatemia Hyperprolinemia Hypersplenism Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy Hypertrophic Osteoarthropathy, Primary, Autosomal Recessive, 1 Hyperuricemia Hypogonadism Hypogonadotropic Hypogonadism Hypogonadotropism Hypopituitarism Hypoplastic Left Heart Syndrome 1 Hypotrichosis Hypoxia Ichthyosis Ichthyosis, Leukocyte Vacuoles, Alopecia, and Sclerosing Cholangitis Ichthyosis Prematurity Syndrome Idiopathic Recurrent Pericarditis Iga Glomerulonephritis Igg4-Related Sclerosing Cholangitis Immune System Disease Immunotactoid Glomerulopathy Inflammatory Bowel Disease Influenza Inherited Metabolic Disorder Insulin-Like Growth Factor I Interstitial Nephritis Intestinal Disease Intestinal Perforation Intracranial Aneurysm Intrahepatic Cholangiocarcinoma Intrahepatic Cholestasis Invasive Aspergillosis Iron Metabolism Disease Iron Overload in Africa Irritable Bowel Syndrome Ischemia Ischemic Optic Neuropathy Isolated Gonadotropin-Releasing Hormone Deficiency Kidney Cortex Necrosis Kindler Syndrome Kniest Dysplasia Kwashiorkor Langerhans Cell Histiocytosis Laryngitis Leiomyosarcoma Leukemia Leukodystrophy, Hypomyelinating, 5 Leukoencephalopathy, Hereditary Diffuse, with Spheroids Lichen Planus Lipase Deficiency, Combined Lipid Metabolism Disorder Lipodystrophy Lipodystrophy, Congenital Generalized, Type 2 Liver Cirrhosis Liver Lipoma Long-Chain 3-Hydroxyacyl-Coa Dehydrogenase Deficiency Lung Disease Lupus Erythematosus Lymphangiomatosis Lymphoma Lysosomal Acid Lipase Deficiency Macrocytic Anemia Malignant Otitis Externa Mallory-Weiss Syndrome Marasmus Marginal Zone B-Cell Lymphoma Meconium Ileus Megaloblastic Anemia Melioidosis Membranoproliferative Glomerulonephritis Meningitis Meningitis and Encephalitis Meralgia Paresthetica Metabolic Acidosis Microphthalmia, Syndromic 1 Microvascular Complications of Diabetes 3 Mitochondrial Disorders Mitochondrial Dna Depletion Syndrome 4a Mixed Connective Tissue Disease Mood Disorder Morbid Obesity Mucinous Cystadenofibroma Mucopolysaccharidosis, Type Vii Mucositis Multiple Mitochondrial Dysfunctions Syndrome 5 Multiple Sclerosis Multiple Symmetrical Lipomatosis Muscular Dystrophy Muscular Dystrophy, Duchenne and Becker Type Myeloproliferative Neoplasm Myotonic Dystrophy Necrotizing Fasciitis Neonatal Jaundice Nephrocalcinosis Nephrogenic Systemic Fibrosis Nephrolithiasis Nephrolithiasis, X-Linked Recessive, with Renal Failure Nervous System Disease Neuraminidase Deficiency Neurenteric Cyst Neuroendocrine Tumor Neuronitis Neuropathy Niemann-Pick Disease Night Blindness Nodular Regenerative Hyperplasia Non-a-E Hepatitis Nonalcoholic Steatohepatitis Nonarteritic Anterior Ischemic Optic Neuropathy Non-Involuting Congenital Hemangioma Null-Cell Leukemia Nutritional Deficiency Disease Obesity-Hypoventilation Syndrome Obstructive Jaundice Occipital Horn Syndrome Ocular Motor Apraxia Opisthorchiasis Oral Erosive Lichen Osteoporotic Fracture Ovarian Disease Overhydrated Hereditary Stomatocytosis Overnutrition Pancreas Disease Pancreatitis Pancreatitis, Hereditary Panniculitis Paraquat Poisoning Paresthesia Pdgfrb-Associated Chronic Eosinophilic Leukemia Pediatric Ulcerative Colitis Peliosis Hepatis Pellagra Peptic Ulcer Disease Pericarditis Periostitis Peritonitis Persistent Idiopathic Facial Pain Pfeiffer Syndrome Phosphorylase Kinase Deficiency Pick Disease of Brain Pituitary Hormone Deficiency, Combined, 2 Pituitary Tumors Placenta Disease Placental Insufficiency Pneumoconiosis Pneumonia Polycystic Kidney Disease Polycystic Kidney Disease 1 Polycystic Kidney Disease 2 Polycystic Kidney Disease 5 Polycystic Liver Disease Polycystic Liver Disease 1 Polycystic Ovary Syndrome Polycythemia Polyembryoma Porokeratosis Porphyria Porphyria Cutanea Tarda Portal Hypertension Portal Vein Thrombosis Prediabetes Syndrome Pre-Eclampsia Primary Biliary Cholangitis Primary Biliary Cirrhosis Primary Hyperoxaluria Prostatitis Protein C Deficiency Protein-Energy Malnutrition Protoporphyria, Erythropoietic Psoriasis Psoriasis 13 Psoriatic Arthritis Pulmonary Hypertension Punctate Porokeratosis Purpura Purpura Fulminans Pyridoxine Deficiency Renal Tubular Acidosis Respiratory System Disease Restless Legs Syndrome Retinitis Reye Syndrome Rheumatic Disease Rheumatoid Arthritis Salt and Pepper Developmental Regression Syndrome Sarcoidosis 2 Scalp-Ear-Nipple Syndrome Schistosomiasis Schizophrenia Schneiderian Carcinoma Sclerosing Cholangitis Scrub Typhus Secondary Sclerosing Cholangitis Secondary Syphilis Serine Deficiency Severe Hemophilia a Short Bowel Syndrome Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis Shwachman-Diamond Syndrome Sialadenitis Sickle Cell Anemia Siderosis Sleep Apnea Spinal and Bulbar Muscular Atrophy, X-Linked 1 Splenic Artery Aneurysm Splenic Disease Splenomegaly Spondyloocular Syndrome Squamous Cell Carcinoma Steatorrhea Substance Abuse Syndrome of Inappropriate Antidiuretic Hormone Syphilis Syringocystadenoma Papilliferum Syringomyelia Systemic Lupus Erythematosus Systemic Mastocytosis Testicular Yolk Sac Tumor Thalassemia Thrombocytopenia Thrombophilia Thrombosis Thyroiditis Timothy Syndrome Treacher Collins Syndrome 1 Trichohepatoenteric Syndrome 1 Trypanosomiasis Tuberculous Peritonitis Tuberous Sclerosis 1 Tuberous Sclerosis 2 Type Ii Mixed Cryoglobulinemia Tyrosinemia Ulcerative Colitis Umbilical Hernia Uremia Van Der Woude Syndrome 1 Vascular Disease Vasculitis Vein Disease Vibrio Vulnificus Infection Viral Hepatitis Virus-Associated Trichodysplasia Spinulosa Werner Syndrome Wilson Disease Xanthomatosis X-Linked Intellectual Disability-Macrocephaly-Macroorchidism Syndrome Zygomycosis