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Xanthomatosis
Informaţii despre
Nume
Xanthomatosis
Pagina Web
www.malacards.org
Clasificare globală Malacards
Boli metabolice
Vezi şi
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
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