Informaţii despre

Nume Lipid Metabolism Disorder
Pagina Web www.malacards.org
Clasificare globală Malacards Boli metabolice
Clasificari ICD10 Disorders of fatty-acid metabolism

Vezi şi

Boli A-Z 3-Hydroxyacyl-Coa Dehydrogenase Deficiency Abdominal Obesity-Metabolic Syndrome 1 Abdominal Obesity-Metabolic Syndrome Quantitative Trait Locus 2 Abetalipoproteinemia Acanthosis Nigricans Acquired Generalized Lipodystrophy Acquired Metabolic Disease Acute Myocardial Infarction Adie Pupil Aging Alcoholic Cardiomyopathy Alopecia, Neurologic Defects, and Endocrinopathy Syndrome Al-Raqad Syndrome Amyloidosis Aa Angina Pectoris Aniridia 1 Anorexia Nervosa 1 Aortic Atherosclerosis Apnea, Obstructive Sleep Apo a-I Deficiency Arcus Corneae Arrhythmogenic Right Ventricular Dysplasia, Familial, 4 Arteries, Anomalies of Arteriosclerosis Arthrochalasia Ehlers-Danlos Syndrome Atherosclerosis Susceptibility Blood Group--Ahonen 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 Bulimia Nervosa 2 Carotid Artery Disease Carotid Stenosis Cerebral Atherosclerosis Cerebrovascular Disease Chanarin-Dorfman Syndrome Chylomicron Retention Disease Congenital Generalized Lipodystrophy Coronary Artery Aneurysm Coronary Artery Anomaly Coronary Heart Disease 1 Coronary Restenosis Coronary Stenosis Defective Apolipoprotein B-100 Diabetes Mellitus Dysbaric Osteonecrosis Endocrine Pancreas Disease Familial Hyperlipidemia Familial Lcat Deficiency Familial Lipoprotein Lipase Deficiency Familial Partial Lipodystrophy Fatty Liver Disease Fetal Macrosomia Fish-Eye Disease Gallbladder Disease Generalized Atherosclerosis Gestational Diabetes Glucose Intolerance Glucose Metabolism Disease Hemorrhage, Intracerebral Hepatic Adenomas, Familial Hepatic Lipase Deficiency Hepatitis Hepatitis C Homozygous Familial Hypercholesterolemia Hyperalphalipoproteinemia 1 Hypercholesterolemia, Autosomal Dominant, Type B Hypercholesterolemia, Familial Hyperglycemia Hyperinsulinism Hyperlipidemia, Combined, 1 Hyperlipidemia, Familial Combined Hyperlipoproteinemia, Type Iii Hyperlipoproteinemia, Type Iv Hyperlipoproteinemia, Type V Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy Hypertensive Retinopathy Hypertriglyceridemia, Familial Hyperuricemia Hypoalphalipoproteinemia, Primary Hypobetalipoproteinemia, Familial, 1 Hypolipoproteinemia Ichthyosis Idiopathic Edema Idiopathic Recurrent Pericarditis Inherited Metabolic Disorder Intermittent Claudication Ischemia Ischemic Heart Disease Lecithin:cholesterol Acyltransferase Deficiency Leukodystrophy, Hypomyelinating, 3 Lipase Deficiency, Combined Lipodystrophy Lipodystrophy, Familial Partial, Type 2 Lipogranulomatosis Lipoprotein Glomerulopathy Logopenic Progressive Aphasia Lutheran Suppressor, X-Linked Malignant Otitis Externa Marek Disease Microvascular Complications of Diabetes 5 Moderate and Severe Traumatic Brain Injury Morbid Obesity Multiple Symmetrical Lipomatosis Nephrotic Syndrome Nonalcoholic Steatohepatitis Obesity-Hypoventilation Syndrome Osteonecrosis Overnutrition Peripheral Artery Disease Peroxisomal Acyl-Coa Oxidase Deficiency Polycystic Ovary Syndrome Prediabetes Syndrome Prostate Cancer Prostatitis Sea-Blue Histiocyte Disease Severe Pre-Eclampsia Sitosterolemia Sleep Apnea Smith-Lemli-Opitz Syndrome Tangier Disease Tay-Sachs Disease Undifferentiated Pleomorphic Sarcoma Uremia Vascular Disease Xanthoma Disseminatum Xanthomatosis