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Nume Xanthomatosis
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Clasificare globală Malacards Boli metabolice

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Boli A-Z Abetalipoproteinemia Acquired Immunodeficiency Syndrome Acute Myocardial Infarction Aging Alport Syndrome, X-Linked Al-Raqad Syndrome Alzheimer Disease 3 Anauxetic Dysplasia 1 Aneurysm Angina Pectoris Aniridia 1 Anorexia Nervosa 1 Aortic Aneurysm Aortic Atherosclerosis Arcus Corneae Arteries, Anomalies of Arteriosclerosis Arthritis Arthrochalasia Ehlers-Danlos Syndrome Ataxia and Polyneuropathy, Adult-Onset Ataxia-Oculomotor Apraxia 3 Atherosclerosis Susceptibility Autism Autism Spectrum Disorder Autonomic Dysfunction Bile Duct Disease Biliary Tract Disease Blastic Plasmacytoid Dendritic Cell Blepharospasm Blood Group--Ahonen Blood Group, I System Bone Fracture Bone Mineral Density Quantitative Trait Locus 15 Bone Mineral Density Quantitative Trait Locus 8 Budd-Chiari Syndrome Carotid Artery Disease Cataract Cerebellar Disease Cerebritis Cerebrotendinous Xanthomatosis Cholangitis Cholelithiasis Cholestasis Cholesterol Ester Storage Disease Citrullinemia, Classic Cleft Larynx, Posterior Coronary Artery Anomaly Coronary Heart Disease 1 Cutaneous T Cell Lymphoma Defective Apolipoprotein B-100 Dementia Dermatitis Diabetes Insipidus Diabetes Mellitus Diarrhea Dystonia Epilepsy Euthyroid Sick Syndrome Familial Hyperlipidemia Fox-Fordyce Disease Gallbladder Cancer Gastric Lymphoma Gingivitis Glomerulonephritis Glycogen Storage Disease Hemorrhage, Intracerebral Hepatic Adenomas, Familial Hepatic Lipase Deficiency Hepatitis Histiocytosis Homozygous Familial Hypercholesterolemia Hyperalphalipoproteinemia 1 Hypercholesterolemia, Autosomal Dominant, 3 Hypercholesterolemia, Autosomal Dominant, Type B Hypercholesterolemia, Autosomal Recessive Hypercholesterolemia, Familial Hyperglobulinemic Purpura Hyperlipidemia, Familial Combined Hyperlipoproteinemia, Type Iii Hyperlipoproteinemia, Type Iv Hyperlipoproteinemia, Type V Hyperprolactinemia Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy Hypertriglyceridemia, Familial Hypertrophic Osteoarthropathy, Primary, Autosomal Recessive, 1 Hypoalphalipoproteinemia, Primary Hypobetalipoproteinemia, Familial, 1 Hypocalcemic Vitamin D-Dependent Rickets Hypolipoproteinemia Immunoglobulin E Concentration, Serum Langerhans Cell Histiocytosis Lecithin:cholesterol Acyltransferase Deficiency Leukodystrophy Leukodystrophy, Hypomyelinating, 3 Lipid Metabolism Disorder Lipid Storage Disease Lipoprotein Glomerulopathy Liver Disease Logopenic Progressive Aphasia Lymphangiectasia, Intestinal Lymphangioleiomyomatosis Lymphedema Lymphoma Lysosomal Acid Lipase Deficiency Marfan Syndrome Multicentric Reticulohistiocytosis Multiple Sclerosis Mycosis Fungoides Myeloma, Multiple Myocardial Infarction Myoclonus Myopathy Nephrocalcinosis Nephrolithiasis Nephrolithiasis, X-Linked Recessive, with Renal Failure Neuropathy Oromandibular Dystonia Pancytopenia Parametritis Paraplegia Polyneuropathy Primary Biliary Cirrhosis Pulmonary Hypertension Purpura Recurrent Acute Pancreatitis Relapsing Polychondritis Retinal Vasculitis Retinitis Rheumatoid Arthritis Rickets Schnyder Corneal Dystrophy Sclerosing Cholangitis Sitosterolemia Smith-Lemli-Opitz Syndrome Spasticity Spastic Paraparesis Subacute Glomerulonephritis Syphilitic Myelopathy Tabes Dorsalis Tangier Disease Temporal Arteritis Tendinitis Thrombocytopenia Vaginitis Van Der Woude Syndrome 1 Vasculitis Xanthoma Disseminatum