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Nume Inherited Metabolic Disorder
Pagina Web www.malacards.org
Clasificare globală Malacards Boli metabolice

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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 Liver Failure Adenosine Deaminase Deficiency Al-Raqad Syndrome Amino Acid Metabolic Disorder Aniridia 1 Anorexia Nervosa 1 Apnea, Obstructive Sleep Arcus Corneae Arteries, Anomalies of Arteriosclerosis Arthrochalasia Ehlers-Danlos Syndrome Atherosclerosis Susceptibility Atransferrinemia Autosomal Recessive Sideroblastic Anemia Beta-Thalassemia Blood Group--Ahonen Carotid Artery Disease Carotid Artery Dissection Cerebral Atherosclerosis Cerebral Palsy Cerebritis Cerebrovascular Disease Ceroid Lipofuscinosis, Neuronal, 1 Ceroid Lipofuscinosis, Neuronal, 11 Ceroid Lipofuscinosis, Neuronal, 2 Ceroid Lipofuscinosis, Neuronal, 3 Charles Bonnet Syndrome Cholesterol Ester Storage Disease Chylomicron Retention Disease Classic Congenital Adrenal Hyperplasia Due to 21-Hydroxylase Deficiency Congenital Disorder of Glycosylation, Type Ii Congenital Generalized Lipodystrophy Coronary Artery Anomaly Coronary Heart Disease 1 Coronary Stenosis Crigler-Najjar Syndrome, Type I Crigler-Najjar Syndrome, Type Ii Cryptogenic Cirrhosis Cystathioninuria Cystic Fibrosis Diffuse Lymphatic Malformation Dihydropyrimidine Dehydrogenase Deficiency Encephalopathy Endocrine Pancreas Disease Epilepsy Ethylene Glycol Poisoning Fabry Disease Familial Hyperlipidemia Fatty Liver Disease Fetal Macrosomia Folic Acid Deficiency Anemia Fucosidosis Gallbladder Disease Gangliosidosis Gm1 Gaucher's Disease Gestational Diabetes Gilbert Syndrome Glucose Intolerance Glucose Metabolism Disease Glycine N-Methyltransferase Deficiency Hematopoietic Stem Cell Transplantation Hemochromatosis, Type 1 Hemochromatosis Type 2 Hemochromatosis, Type 3 Hemoglobinopathy Hemosiderosis Hfe-Associated Hereditary Hemochromatosis Homocysteinemia Homocystinuria Hypercholesterolemia, Familial Hyperferritinemia with or Without Cataract Hyperglycemia Hyperinsulinism Hyperlipidemia, Familial Combined Hyperlipoproteinemia, Type Iii Hypertriglyceridemia, Familial Hyperuricemia Hypobetalipoproteinemia, Familial, 1 Idiopathic Recurrent Pericarditis Iron Metabolism Disease Iron Overload in Africa Kernicterus Lactic Acidosis Lens Subluxation Leukodystrophy, Hypomyelinating, 3 Lipid Metabolism Disorder Lipid Storage Disease Lipodystrophy Lipodystrophy, Familial Partial, Type 2 Liver Cirrhosis Liver Disease Lutheran Suppressor, X-Linked Lysosomal Storage Disease Malignant Otitis Externa Mannosidosis, Alpha B, Lysosomal Mastoiditis Mediastinitis Melancholia Metachromatic Leukodystrophy Metal Metabolism Disorder Methylmalonic Aciduria and Homocystinuria, Cblc Type Mitochondrial Myopathy Miyoshi Muscular Dystrophy 1 Morbid Obesity Mucopolysaccharidosis-Plus Syndrome Mucopolysaccharidosis, Type Ii Mucopolysaccharidosis Type Vi Mucopolysaccharidosis, Type Vii Multiple Sulfatase Deficiency Myopathy Neuropathy Nonalcoholic Steatohepatitis Nutritional Deficiency Disease Obesity-Hypoventilation Syndrome Overnutrition Peripheral Artery Disease Phenylketonuria Pigmentation Disease Polycystic Ovary Syndrome Porphyria Porphyria Cutanea Tarda Porphyria Variegata Precocious Puberty Prediabetes Syndrome Progressive Bulbar Palsy Pulmonary Hypertension, Primary, 1 Riboflavin Deficiency Sandhoff Disease Scheie Syndrome Sickle Cell Anemia Siderosis Sleep Apnea Sleep Disorder Sphingolipidosis Tangier Disease Testicular Yolk Sac Tumor Thalassemia Urea Cycle Disorder Uremia Vascular Disease Wilson Disease