Informaţii despre

Nume Hypercholesterolemia, Familial
Pagina Web www.malacards.org
Clasificare globală Malacards Boli genetice; Boli metabolice; Boli rare
Clasificari ICD10 Pure hypercholesterolaemia
Boli din aceeaşi familie Hypercholesterolemia, Autosomal Dominant, 3; Hypercholesterolemia, Autosomal Dominant, Type B; Hypercholesterolemia, Autosomal Recessive

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Boli A-Z Abetalipoproteinemia Ablepharon-Macrostomia Syndrome Acrocallosal Syndrome Acute Myocardial Infarction Aging Aland Island Eye Disease Alopecia, Neurologic Defects, and Endocrinopathy Syndrome Alport Syndrome, X-Linked Al-Raqad Syndrome Alzheimer Disease 3 Amyloidosis Aa Amyloidosis, Familial Visceral Anauxetic Dysplasia 1 Aneurysm Angel-Shaped Phalangoepiphyseal Dysplasia Aniridia 1 Anorexia Nervosa 1 Aortic Atherosclerosis Apo a-I Deficiency Apolipoprotein C-Ii Deficiency Apparent Mineralocorticoid Excess Arcus Corneae Arrhythmogenic Right Ventricular Dysplasia, Familial, 4 Arterial Calcification, Generalized, of Infancy, 1 Arteries, Anomalies of Arteriosclerosis Arteriovenous Fistula Arthritis Arthrochalasia Ehlers-Danlos Syndrome Atherosclerosis Susceptibility Beta-Thalassemia Blood Group--Ahonen Blood Group, Dombrock System Blood Group, I System Bursitis Cardiomyopathy, Familial Hypertrophic, 1 Carotenemia Carotid Artery Disease Carotid Artery Thrombosis Carotid Stenosis Cerebral Atherosclerosis Cerebritis Cerebrotendinous Xanthomatosis Cerebrovascular Disease Cholelithiasis Cholesterol Ester Storage Disease Chronic Progressive External Ophthalmoplegia Chylomicron Retention Disease Coarctation of Aorta Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy Coronary Aneurysm Coronary Artery Anomaly Coronary Heart Disease 1 Coronary Stenosis Defective Apolipoprotein B-100 Diabetes Mellitus Dilated Cardiomyopathy Endotheliitis Factor X Deficiency Familial Hyperlipidemia Familial Lcat Deficiency Familial Lipoprotein Lipase Deficiency Fetal Macrosomia Fish-Eye Disease Floating-Harbor Syndrome Focal Segmental Glomerulosclerosis Gallbladder Disease Hepatic Adenomas, Familial Hepatic Lipase Deficiency Hepatitis Hinman Syndrome Homocystinuria Homozygous Familial Hypercholesterolemia Huntington Disease-Like 3 Hyperalphalipoproteinemia 1 Hypercholesterolemia, Autosomal Dominant, 3 Hypercholesterolemia, Autosomal Dominant, Type B Hypercholesterolemia, Autosomal Recessive Hyperlipidemia, Familial Combined Hyperlipoproteinemia, Type Iii Hyperlipoproteinemia, Type Iv Hyperlipoproteinemia, Type V Hyperthyroxinemia Hypertriglyceridemia, Familial Hypertrophic Cardiomyopathy Hypertrophic Osteoarthropathy, Primary, Autosomal Recessive, 1 Hyperuricemia Hypoalphalipoproteinemia, Primary Hypobetalipoproteinemia, Familial, 1 Hypolipoproteinemia Immunoglobulin E Concentration, Serum Ischemia Ischemic Heart Disease Lateral Myocardial Infarction Lecithin:cholesterol Acyltransferase Deficiency Left Ventricular Noncompaction Leukodystrophy, Hypomyelinating, 3 Leukoencephalopathy, Hereditary Diffuse, with Spheroids Lipase Deficiency, Combined Lipid Metabolism Disorder Lipomatosis Lipoprotein Glomerulopathy Logopenic Progressive Aphasia Lowe Oculocerebrorenal Syndrome Lung Cancer Lysosomal Acid Lipase Deficiency Malignant Otitis Externa Middle Ear Cholesterol Granuloma Mungan Syndrome Myelophthisic Anemia Myocardial Infarction Myxedema Nephrotic Syndrome Niemann-Pick Disease Obstructive Jaundice Periodontitis Peripheral Artery Disease Peripheral Vascular Disease Prediabetes Syndrome Progressive External Ophthalmoplegia with Mitochondrial Dna Deletions, Autosomal Dominant 2 Progressive External Ophthalmoplegia with Mitochondrial Dna Deletions, Autosomal Dominant 3 Progressive External Ophthalmoplegia with Mitochondrial Dna Deletions, Autosomal Dominant 4 Pseudoxanthoma Elasticum Renal Glucosuria Rheumatoid Arthritis Salt and Pepper Developmental Regression Syndrome Schnyder Corneal Dystrophy Sea-Blue Histiocyte Disease Sitosterolemia Smith-Lemli-Opitz Syndrome Splenic Abscess Spondyloocular Syndrome Supravalvular Aortic Stenosis Tangier Disease Taqi Polymorphism Tendinitis Thalassemia Thrombosis Treacher Collins Syndrome 1 Uremia Van Der Woude Syndrome 1 Vascular Disease Vitamin E, Familial Isolated Deficiency of Xanthoma Disseminatum Xanthomatosis