Informaţii despre

Nume Hyperlipidemia, Familial Combined
Pagina Web www.malacards.org
Clasificare globală Malacards Boli genetice; Boli metabolice
Clasificari ICD10 Mixed hyperlipidaemia; Other hyperlipidaemia
Boli din aceeaşi familie Hyperlipidemia, Combined, 1; Hyperlipidemia, Combined, 2

Vezi şi

Boli A-Z Abetalipoproteinemia Aging Aland Island Eye Disease Alopecia, Neurologic Defects, and Endocrinopathy Syndrome Al-Raqad Syndrome Aniridia 1 Anorexia Nervosa 1 Apolipoprotein C-Iii Deficiency Arcus Corneae Arteries, Anomalies of Arteriosclerosis Arthrochalasia Ehlers-Danlos Syndrome Atherosclerosis Susceptibility Blood Group--Ahonen 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 Artery Anomaly Coronary Heart Disease 1 Coronary Stenosis Defective Apolipoprotein B-100 Diabetes Mellitus Dysbaric Osteonecrosis Endotheliitis Familial Hyperlipidemia Familial Lcat Deficiency Familial Lipoprotein Lipase Deficiency Fatty Liver Disease Gallbladder Disease Gastric Antral Vascular Ectasia Hemorrhage, Intracerebral Hepatic Lipase Deficiency Hepatitis Homozygous Familial Hypercholesterolemia Hyperalphalipoproteinemia 1 Hypercholesterolemia, Autosomal Dominant, 3 Hypercholesterolemia, Autosomal Dominant, Type B Hypercholesterolemia, Familial Hyperlipidemia, Combined, 1 Hyperlipoproteinemia, Type Iii Hyperlipoproteinemia, Type Iv Hyperlipoproteinemia, Type V Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy Hypertriglyceridemia, Familial Hypertrophic Osteoarthropathy, Primary, Autosomal Recessive, 1 Hypoalphalipoproteinemia, Primary Hypobetalipoproteinemia, Familial, 1 Hypolipoproteinemia Lecithin:cholesterol Acyltransferase Deficiency Leukodystrophy, Hypomyelinating, 3 Leukoencephalopathy, Hereditary Diffuse, with Spheroids Lipid Metabolism Disorder Lipoprotein Glomerulopathy Liver Disease Myocardial Infarction Nuchal Bleb, Familial Otosclerosis Pituitary Hormone Deficiency, Combined, 2 Recurrent Acute Pancreatitis Retinitis Salt and Pepper Developmental Regression Syndrome Schnyder Corneal Dystrophy Sitosterolemia Smith-Lemli-Opitz Syndrome Tangier Disease Vitamin E, Familial Isolated Deficiency of Xanthoma Disseminatum Xanthomatosis