Informaţii despre

Nume Hypertriglyceridemia, Transient Infantile
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Clasificare globală Malacards Boli genetice; Boli rare
Clasificare anatomică Malacards Boli hepatice

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Boli A-Z Acanthosis Nigricans Acquired Immunodeficiency Syndrome Acute Lymphocytic Leukemia Acute Pancreatitis Acute Promyelocytic Leukemia Adenoma Aging Aland Island Eye Disease Alopecia, Neurologic Defects, and Endocrinopathy Syndrome 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 Aphthous Stomatitis Apnea, Obstructive Sleep Apolipoprotein C-Ii Deficiency Apolipoprotein C-Iii Deficiency Arteries, Anomalies of Arthrochalasia Ehlers-Danlos Syndrome 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 Stenosis Cerebritis Chediak-Higashi Syndrome Colitis Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy Cystic Fibrosis Diabetes Mellitus Diabetes Mellitus, Noninsulin-Dependent Diabetic Macular Edema Donnai-Barrow Syndrome Endometrial Cancer Endotheliitis Epithelial Recurrent Erosion Dystrophy Facial Paralysis Familial Hyperlipidemia Familial Lipoprotein Lipase Deficiency Familial Partial Lipodystrophy Fatty Liver Disease Fructose-1,6-Bisphosphatase Deficiency Gestational Diabetes Glucose Intolerance Glycogen Storage Disease Gout Helix Syndrome Hemophagocytic Lymphohistiocytosis Hepatic Adenomas, Familial Hepatitis Hepatitis B Hinman Syndrome Homocystinuria Due to Deficiency of N -Methylenetetrahydrofolate Reductase Activity Hydrops, Lactic Acidosis, and Sideroblastic Anemia Hyperalphalipoproteinemia 1 Hypercholesterolemia, Autosomal Dominant, 3 Hyperglycemia Hyperinsulinism Hyperlipidemia, Combined, 2 Hyperlipidemia, Familial Combined Hyperlipoproteinemia, Type Iv Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy Hypertriglyceridemia, Familial Hypertrophic Osteoarthropathy, Primary, Autosomal Recessive, 1 Hyperuricemia Hypoalphalipoproteinemia, Primary Hypoglycemia Hypophosphatemia Hypoxia Lactic Acidosis Leukemia Leukoencephalopathy, Hereditary Diffuse, with Spheroids Lipodystrophy Lipodystrophy, Congenital Generalized, Type 2 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 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