Informaţii despre

Nume Hypertriglyceridemia, Familial
Pagina Web www.malacards.org
Clasificare globală Malacards Boli genetice; Boli rare
Clasificare anatomică Malacards Boli hepatice
Boli din aceeaşi familie Hypertriglyceridemia, Transient Infantile

Vezi şi

Boli A-Z Abetalipoproteinemia Acanthosis Nigricans Acquired Immunodeficiency Syndrome Acute Lymphocytic Leukemia Acute Pancreatitis Acute Promyelocytic Leukemia Adenoma Aging Aland Island Eye Disease Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity Alport Syndrome, X-Linked Al-Raqad Syndrome Aniridia 1 Anorexia Nervosa 1 Aortic Atherosclerosis Aphthous Stomatitis Apnea, Obstructive Sleep Apolipoprotein C-Ii Deficiency Apolipoprotein C-Iii Deficiency Arcus Corneae Arteries, Anomalies of Arteriosclerosis Arthrochalasia Ehlers-Danlos Syndrome Atherosclerosis Susceptibility Autoimmune Disease Biliary Dyskinesia 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 Mineral Density Quantitative Trait Locus 15 Bone Mineral Density Quantitative Trait Locus 8 Brain Injury Breast Cancer Cardiac Arrest Carotid Artery Disease Carotid Stenosis Cerebral Atherosclerosis Cerebritis Cerebrovascular Disease Chediak-Higashi Syndrome Chylomicron Retention Disease Colitis Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy Coronary Artery Anomaly Coronary Heart Disease 1 Coronary Stenosis Cystic Fibrosis Defective Apolipoprotein B-100 Diabetes Mellitus Diabetes Mellitus, Noninsulin-Dependent Diabetic Macular Edema Donnai-Barrow Syndrome Dysbaric Osteonecrosis Endometrial Cancer Endotheliitis Epithelial Recurrent Erosion Dystrophy Facial Paralysis Familial Hyperlipidemia Familial Lcat Deficiency Familial Lipoprotein Lipase Deficiency Familial Partial Lipodystrophy Fatty Liver Disease Fetal Macrosomia Fructose-1,6-Bisphosphatase Deficiency Gallbladder Disease Gestational Diabetes Glucose Intolerance Glycogen Storage Disease Gout Helix Syndrome Hemophagocytic Lymphohistiocytosis Hepatic Adenomas, Familial Hepatic Lipase Deficiency Hepatitis Hepatitis B Hinman Syndrome Homocystinuria Due to Deficiency of N -Methylenetetrahydrofolate Reductase Activity Homozygous Familial Hypercholesterolemia Hydrops, Lactic Acidosis, and Sideroblastic Anemia Hyperalphalipoproteinemia 1 Hypercholesterolemia, Autosomal Dominant, 3 Hypercholesterolemia, Autosomal Dominant, Type B Hypercholesterolemia, Familial Hyperglycemia Hyperinsulinism Hyperlipidemia, Combined, 2 Hyperlipidemia, Familial Combined Hyperlipoproteinemia, Type Iii Hyperlipoproteinemia, Type Iv Hyperlipoproteinemia, Type V Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy Hypertriglyceridemia, Transient Infantile Hypertrophic Osteoarthropathy, Primary, Autosomal Recessive, 1 Hyperuricemia Hypoalphalipoproteinemia, Primary Hypobetalipoproteinemia, Familial, 1 Hypoglycemia Hypolipoproteinemia Hypophosphatemia Hypoxia Lactic Acidosis Lecithin:cholesterol Acyltransferase Deficiency Leukemia Leukodystrophy, Hypomyelinating, 3 Leukoencephalopathy, Hereditary Diffuse, with Spheroids Lipase Deficiency, Combined Lipid Metabolism Disorder Lipodystrophy Lipodystrophy, Congenital Generalized, Type 2 Lipoprotein Glomerulopathy Liver Cirrhosis Liver Disease Lung Cancer Lupus Erythematosus Lymphoblastic Leukemia Lymphoma Melanoma Metabolic Acidosis Microcolon Mucopolysaccharidosis-Plus Syndrome Mucopolysaccharidosis Type Vi Mungan Syndrome Myocardial Infarction Neonatal Diabetes Mellitus Nephrotic Syndrome Neuropathy Pancreatitis Pancytopenia Periodontal Disease Periodontitis Peritonitis Polydactyly, Postaxial, with Progressive Myopia Polyneuropathy Polyradiculopathy Portal Hypertension Prediabetes Syndrome Priapism Prostate Cancer Prostatitis Protein-Losing Enteropathy Recurrent Acute Pancreatitis Salt and Pepper Developmental Regression Syndrome Scalp-Ear-Nipple Syndrome Schnyder Corneal Dystrophy Splenomegaly Spotted Fever Stomatitis Syringocystadenoma Papilliferum Systemic Lupus Erythematosus Tangier Disease Thalassemia Thrombocytopenia Thrombosis Uremia Vascular Disease Vitamin E, Familial Isolated Deficiency of Werner Syndrome Xanthoma Disseminatum Xanthomatosis