Informaţii despre

Nume Lecithin:cholesterol Acyltransferase Deficiency
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 nefrologice (ale rinichilor)

Vezi şi

Boli A-Z Abetalipoproteinemia Acute Pancreatitis Alcoholic Hepatitis Al-Raqad Syndrome Amyloidosis Aa Amyloidosis, Familial Visceral Aniridia 1 Anorexia Nervosa 1 Aortic Atherosclerosis Apo a-I Deficiency Apolipoprotein C-Ii Deficiency Arcus Corneae Arrhythmogenic Right Ventricular Dysplasia, Familial, 4 Arteries, Anomalies of Arteriosclerosis Arthrochalasia Ehlers-Danlos Syndrome Atherosclerosis Susceptibility Blood Group--Ahonen Blood Group, I System Bloom Syndrome 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 Carotid Artery Disease Cerebral Atherosclerosis Cerebrovascular Disease Chylomicron Retention Disease Coronary Artery Anomaly Coronary Heart Disease 1 Coronary Stenosis Cutis Laxa, Autosomal Recessive, Type Iiia Defective Apolipoprotein B-100 Diabetes Mellitus Ewing Sarcoma Familial Hyperlipidemia Familial Lcat Deficiency Familial Lipoprotein Lipase Deficiency Fetal Macrosomia Fish-Eye Disease Gallbladder Disease Glomerulonephritis Hemolytic Anemia Hepatic Lipase Deficiency Hepatitis Hereditary Amyloidosis Histiocytosis Homozygous Familial Hypercholesterolemia Hyperalphalipoproteinemia 1 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 Hypolipoproteinemia Kwashiorkor Leukodystrophy, Hypomyelinating, 3 Leukoencephalopathy, Hereditary Diffuse, with Spheroids Lipid Metabolism Disorder Lipoprotein Glomerulopathy Logopenic Progressive Aphasia Membranoproliferative Glomerulonephritis Pancreatitis Recurrent Acute Pancreatitis Sarcoidosis 2 Schnyder Corneal Dystrophy Sea-Blue Histiocyte Disease Smith-Lemli-Opitz Syndrome Splenomegaly Tangier Disease Uremia Xanthoma Disseminatum Xanthomatosis