Informaţii despre

Nume Hypoalphalipoproteinemia, Primary
Pagina Web www.malacards.org
Clasificare globală Malacards Boli genetice; Boli metabolice; Boli rare
Clasificari ICD10 Lipoprotein deficiency
Clasificare anatomică Malacards Boli endocrine

Vezi şi

Boli A-Z Abetalipoproteinemia Adie Pupil Aging Aland Island Eye Disease Alopecia, Neurologic Defects, and Endocrinopathy Syndrome Alport Syndrome, X-Linked Al-Raqad Syndrome Amyloidosis Amyloidosis Aa Aniridia 1 Anorexia Nervosa 1 Aortic Atherosclerosis Apo a-I Deficiency Arcus Corneae Arteries, Anomalies of Arthrochalasia Ehlers-Danlos Syndrome Atherosclerosis Susceptibility Blood Group--Ahonen 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 Chylomicron Retention Disease Coronary Artery Anomaly Coronary Heart Disease 1 Coronary Stenosis Defective Apolipoprotein B-100 Dysbaric Osteonecrosis Endotheliitis Familial Hyperlipidemia Familial Lcat Deficiency Familial Lipoprotein Lipase Deficiency Fetal Macrosomia Fish-Eye Disease Gallbladder Disease Hepatic Adenomas, Familial Hepatic Lipase Deficiency Hepatitis Hereditary Amyloidosis High Density Lipoprotein Cholesterol Level Quantitative Trait Locus 14 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 Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy Hypertriglyceridemia, Familial Hypobetalipoproteinemia, Familial, 1 Hypolipoproteinemia Lecithin:cholesterol Acyltransferase Deficiency Leukodystrophy, Hypomyelinating, 3 Leukoencephalopathy, Hereditary Diffuse, with Spheroids Lipase Deficiency, Combined Lipid Metabolism Disorder Lipoprotein Glomerulopathy Lowe Oculocerebrorenal Syndrome Peroxisomal Acyl-Coa Oxidase Deficiency Salt and Pepper Developmental Regression Syndrome Sarcoidosis 2 Schnyder Corneal Dystrophy Smith-Lemli-Opitz Syndrome Tangier Disease Vitamin E, Familial Isolated Deficiency of Xanthomatosis