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Boli A-Z Abetalipoproteinemia Amyloidosis Aa Amyloidosis, Familial Visceral Aortic Atherosclerosis Arcus Corneae Arteries, Anomalies of Arteriosclerosis Arthrochalasia Ehlers-Danlos Syndrome Atherosclerosis Susceptibility Carotid Artery Disease Cerebral Atherosclerosis Cerebrovascular Disease Chylomicron Retention Disease Coronary Artery Anomaly Coronary Heart Disease 1 Coronary Stenosis Defective Apolipoprotein B-100 Dysbaric Osteonecrosis Familial Hyperlipidemia Familial Lcat Deficiency Fetal Macrosomia Fish-Eye Disease Gallbladder Disease Hepatic Adenomas, Familial Hepatic Lipase Deficiency Hereditary Amyloidosis Homozygous Familial Hypercholesterolemia Hyperalphalipoproteinemia 1 Hypercholesterolemia, Autosomal Dominant, Type B Hypercholesterolemia, Familial Hyperlipidemia, Familial Combined Hyperlipoproteinemia, Type Iii Hyperlipoproteinemia, Type Iv Hypertriglyceridemia, Familial Hypoalphalipoproteinemia, Primary Hypobetalipoproteinemia, Familial, 1 Hypolipoproteinemia Hypomyelinating Leukodystrophy Lecithin:cholesterol Acyltransferase Deficiency Leukodystrophy Leukodystrophy, Hypomyelinating, 10 Leukodystrophy, Hypomyelinating, 11 Leukodystrophy, Hypomyelinating, 12 Leukodystrophy, Hypomyelinating, 13 Leukodystrophy, Hypomyelinating, 2 Leukodystrophy, Hypomyelinating, 4 Leukodystrophy, Hypomyelinating, 5 Leukodystrophy, Hypomyelinating, 6 Leukodystrophy, Hypomyelinating, 7, with or Without Oligodontia and/or Hypogonadotropic Hypogonadism Leukodystrophy, Hypomyelinating, 9 Lipid Metabolism Disorder Lipoprotein Glomerulopathy Logopenic Progressive Aphasia Microphthalmia, Syndromic 9 Pelizaeus-Merzbacher Disease Pelizaeus-Merzbacher-Like Disease Persistent Mullerian Duct Syndrome, Types I and Ii Schnyder Corneal Dystrophy Spasticity Sphingolipidosis Tangier Disease Tetraamelia Syndrome, Autosomal Recessive Vitamin E, Familial Isolated Deficiency of Xanthoma Disseminatum Xanthomatosis