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