Informaţii despre

Nume Hypobetalipoproteinemia, Familial, 1
Pagina Web www.malacards.org
Clasificare globală Malacards Boli genetice; Boli metabolice
Boli din aceeaşi familie Hypobetalipoproteinemia, Familial, 2

Vezi şi

Boli A-Z Abetalipoproteinemia Afibrinogenemia Aging Alopecia, Neurologic Defects, and Endocrinopathy Syndrome Alport Syndrome, X-Linked Al-Raqad Syndrome Amyloidosis Aa 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 Atherosclerosis Susceptibility Blood Group--Ahonen Blood Group, Dombrock System Blood Group, I System 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 Heart Disease 1 Coronary Stenosis Defective Apolipoprotein B-100 Diabetes Mellitus Dysbaric Osteonecrosis Familial Hyperlipidemia Familial Lcat Deficiency Fanconi Anemia, Complementation Group E Fatty Liver Disease Fatty Liver Disease, Nonalcoholic 1 Fetal Macrosomia Fish-Eye Disease Gallbladder Disease Hepatic Lipase Deficiency Hepatitis Hepatitis C Hepatitis C Virus Hepatocellular Carcinoma Hereditary Spastic Paraplegia Homozygous Familial Hypercholesterolemia Hyperalphalipoproteinemia 1 Hypercholesterolemia, Autosomal Dominant, Type B Hypercholesterolemia, Familial Hyperlipidemia, Familial Combined Hyperlipoproteinemia, Type I Hyperlipoproteinemia, Type Iii Hyperlipoproteinemia, Type Iv Hypertriglyceridemia, Familial Hypoalphalipoproteinemia, Primary Hypolipoproteinemia Lecithin:cholesterol Acyltransferase Deficiency Leukodystrophy, Hypomyelinating, 3 Lipid Metabolism Disorder Lipoprotein Glomerulopathy Liver Disease Mast Cell Activation Syndrome Muscular Atrophy Neuropathy Nguyen Syndrome Nonalcoholic Steatohepatitis Paraplegia Primary Cerebellar Degeneration Retinal Degeneration Retinitis Retinitis Pigmentosa Rickets Schnyder Corneal Dystrophy Sea-Blue Histiocyte Disease Sitosterolemia Smith-Lemli-Opitz Syndrome Spasticity Spinal Muscular Atrophy Spinocerebellar Degeneration Steatorrhea Tangier Disease Vitamin E, Familial Isolated Deficiency of Xanthoma Disseminatum Xanthomatosis