Informaţii despre

Nume Abetalipoproteinemia
Pagina Web www.malacards.org
Clasificare globală Malacards Boli genetice; Boli metabolice; Boli rare
Clasificari ICD10 Lipoprotein deficiency
Clasificare anatomică Malacards Boli ale ochiului; Boli de sânge; Boli endocrine; Boli gastrointestinale; Boli neuronale

Vezi şi

Boli A-Z Acrodermatitis Adenocarcinoma Adie Pupil Alopecia, Neurologic Defects, and Endocrinopathy Syndrome Al-Raqad Syndrome Angioid Streaks Aniridia 1 Anorexia Nervosa 1 Aortic Atherosclerosis Apo a-I Deficiency Arcus Corneae Arteries, Anomalies of Arteriosclerosis Arthrochalasia Ehlers-Danlos Syndrome Ataxia and Polyneuropathy, Adult-Onset Ataxia Neuropathy Spectrum Ataxia with Vitamin E Deficiency Atherosclerosis Susceptibility Blood Group--Ahonen Blood Group, I System Carotid Artery Disease Cerebral Atherosclerosis Cerebrovascular Disease Chorioretinitis Chylomicron Retention Disease Coronary Artery Anomaly Coronary Heart Disease 1 Coronary Stenosis Defective Apolipoprotein B-100 Diabetes Mellitus Diarrhea Dubin-Johnson Syndrome Enteropathica Familial Hyperlipidemia Familial Lcat Deficiency Fanconi Anemia, Complementation Group E Fatty Liver Disease Fetal Macrosomia Fish-Eye Disease Gallbladder Disease Glioblastoma Hepatic Adenomas, Familial Hepatic Lipase Deficiency Hepatitis Hereditary Spastic Paraplegia Homozygous Familial Hypercholesterolemia Hyperalphalipoproteinemia 1 Hypercholesterolemia, Autosomal Dominant, 3 Hypercholesterolemia, Autosomal Dominant, Type B Hypercholesterolemia, Familial Hyperlipidemia, Familial Combined Hyperlipoproteinemia, Type Iii Hyperlipoproteinemia, Type Iv Hyperlipoproteinemia, Type V Hypertriglyceridemia, Familial Hypoalphalipoproteinemia, Primary Hypobetalipoproteinemia, Familial, 1 Hypogonadism Hypolipoproteinemia Lecithin:cholesterol Acyltransferase Deficiency Leukodystrophy, Hypomyelinating, 3 Leukoencephalopathy, Hereditary Diffuse, with Spheroids Lipid Metabolism Disorder Lipoprotein Glomerulopathy Liver Disease Long-Chain 3-Hydroxyacyl-Coa Dehydrogenase Deficiency Mast Cell Activation Syndrome Mitochondrial Trifunctional Protein Deficiency Myopathy Neuropathy Nguyen Syndrome Nonalcoholic Steatohepatitis Paraplegia Pneumonia Premature Ovarian Failure 1 Recurrent Acute Pancreatitis Retinal Degeneration Retinitis Retinitis Pigmentosa Rickets Schnyder Corneal Dystrophy Sea-Blue Histiocyte Disease Sitosterolemia Spasticity Sveinsson Chorioretinal Atrophy Tangier Disease Tetraamelia Syndrome, Autosomal Recessive Tremor Vitamin E, Familial Isolated Deficiency of Xanthoma Disseminatum Xanthomatosis X-Linked Intellectual Disability-Macrocephaly-Macroorchidism Syndrome