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

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Boli A-Z Abetalipoproteinemia Ablepharon-Macrostomia Syndrome Acrocallosal Syndrome Acute Myocardial Infarction Adiposis Dolorosa Aging Alagille Syndrome 1 Aland Island Eye Disease Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity Alport Syndrome, X-Linked Al-Raqad Syndrome Alzheimer Disease 3 Analbuminemia Anauxetic Dysplasia 1 Anencephaly Aneurysm Angel-Shaped Phalangoepiphyseal Dysplasia Aniridia 1 Anorexia Nervosa 1 Aortic Atherosclerosis Apolipoprotein C-Iii Deficiency Apparent Mineralocorticoid Excess Arcus Corneae Arterial Calcification, Generalized, of Infancy, 1 Arteries, Anomalies of Arteriosclerosis Arteriovenous Fistula Arthritis Arthrochalasia Ehlers-Danlos Syndrome Arthrogryposis, Renal Dysfunction, and Cholestasis 1 Asperger Syndrome Ataxia and Polyneuropathy, Adult-Onset Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus Ataxia-Telangiectasia Azoospermia Beta-Thalassemia Bleeding Disorder, Platelet-Type, 11 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 Breast Cancer Bursitis Cardiac Arrhythmia Carotid Artery Thrombosis Carotid Intimal Medial Thickness 2 Carotid Stenosis Cerebral Atherosclerosis Cerebritis Cerebrotendinous Xanthomatosis Cerebrovascular Disease Cholangiocarcinoma Cholelithiasis Cholestasis Cholesterol Ester Storage Disease Choroiditis Chronic Graft Versus Host Disease Chronic Myocardial Ischemia Chronic Progressive External Ophthalmoplegia Coarctation of Aorta Colorectal Cancer Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy Congenital Analbuminemia Coronary Aneurysm Coronary Stenosis Defective Apolipoprotein B-100 Dementia Diabetes Mellitus Dilated Cardiomyopathy Endotheliitis Eosinophilic Gastroenteritis Epilepsy Epithelial Recurrent Erosion Dystrophy Factor X Deficiency Familial Hyperlipidemia Floating-Harbor Syndrome Focal Segmental Glomerulosclerosis Fontaine Progeroid Syndrome Gastroenteritis Glaucoma-Related Pigment Dispersion Syndrome Glucose Intolerance Glycogen Storage Disease Graft-Versus-Host Disease Granulomatous Hepatitis Hepatic Adenomas, Familial Hepatitis Hepatocellular Carcinoma Hinman Syndrome Homocysteinemia Homocystinuria Homozygous Familial Hypercholesterolemia Huntington Disease-Like 3 Hyperaldosteronism, Familial, Type Iii Hyperalphalipoproteinemia 1 Hypercholesterolemia, Autosomal Dominant, Type B Hypercholesterolemia, Autosomal Recessive Hypercholesterolemia, Familial Hyperglycemia Hyperlipidemia, Familial Combined Hyperlipoproteinemia, Type Iv Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy Hyperthyroxinemia Hypertrophic Cardiomyopathy Hypertrophic Osteoarthropathy, Primary, Autosomal Recessive, 1 Hyperuricemia Hypoparathyroidism, Sensorineural Deafness, and Renal Disease Hypopituitarism Hypoxia Immunoglobulin E Concentration, Serum Ischemia Kagami-Ogata Syndrome Kaufman Oculocerebrofacial Syndrome Keratopathy Lateral Myocardial Infarction Left Ventricular Noncompaction Leukoencephalopathy, Hereditary Diffuse, with Spheroids Lipomatosis Liver Disease Lung Cancer Lyme Disease Lysosomal Acid Lipase Deficiency Middle Ear Cholesterol Granuloma Migraine with or Without Aura 1 Multiple Mitochondrial Dysfunctions Syndrome 5 Mungan Syndrome Myelophthisic Anemia Myocardial Infarction Myxedema Nephrotic Syndrome Neuronitis Obstructive Jaundice Opisthorchiasis Pancreatic Cancer Pancreatitis Periodontitis Peripheral Artery Disease Pityriasis Rubra Pilaris Porphyria Prediabetes Syndrome Primary Biliary Cirrhosis 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 Prostate Cancer Prostatitis Pseudoxanthoma Elasticum Psoriasis Psoriasis 13 Psoriatic Arthritis Relapsing Fever Renal Glucosuria Renovascular Hypertension Retinitis Rheumatoid Arthritis Salt and Pepper Developmental Regression Syndrome Scleredema Sensorineural Hearing Loss Sitosterolemia Smith-Magenis Syndrome Spindle Cell Hemangioma Spondyloocular Syndrome Sudden Sensorineural Hearing Loss Supravalvular Aortic Stenosis Taqi Polymorphism Tendinitis Thalassemia Thrombosis Thyroiditis Treacher Collins Syndrome 1 Van Der Woude Syndrome 1 Vascular Disease Xanthomatosis Yemenite Deaf-Blind Hypopigmentation Syndrome