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Nume Amyloidosis
Pagina Web www.malacards.org
Clasificare globală Malacards Genetic diseases; Metabolic diseases; Rare diseases
Clasificari ICD10 Amyloidosis, unspecified
Clasificare anatomică Malacards Blood diseases; Bone diseases; Immune diseases; Nephrological diseases; Neuronal diseases
Boli din aceeaşi familie Ah Amyloidosis; Al Amyloidosis; Amyloidosis Aa; Hereditary Amyloidosis; Primary Localized Amyloidosis

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Boli A-Z 3-Hydroxyacyl-Coa Dehydrogenase Deficiency Aapoai Amyloidosis Aapoaii Amyloidosis Aarskog-Scott Syndrome Abdominal Tuberculosis Acanthosis Nigricans Achalasia Acquired Cutis Laxa Acquired Metabolic Disease Acquired Von Willebrand Syndrome Acromegaly Actinic Keratosis Acute Liver Failure Acute Myocarditis Acute Respiratory Distress Syndrome Adenocarcinoma Adenoma Adrenal Carcinoma Adrenal Hypoplasia, Congenital Adult T-Cell Leukemia Afib Amyloidosis Afibrinogenemia, Congenital Agammaglobulinemia Aging Ah Amyloidosis Alagille Syndrome 1 Al Amyloidosis Aland Island Eye Disease Alect2 Amyloidosis Alkaptonuria Alopecia Alopecia Areata Alopecia, Neurologic Defects, and Endocrinopathy Syndrome Alpha-2-Plasmin Inhibitor Deficiency Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity Alport Syndrome, X-Linked Al-Raqad Syndrome Alternating Hemiplegia of Childhood Alzheimer Disease Alzheimer Disease 2 Alzheimer Disease 3 Alzheimer Disease 4 Ameloblastoma Amyloid Neuropathy Amyloidosis Aa Amyloidosis Beta2m Amyloidosis Cutis Dyschromia Amyloidosis, Familial Visceral Amyloidosis, Finnish Type Amyloidosis, Hereditary, Transthyretin-Related Amyloid Tumor Anauxetic Dysplasia 1 Androgen Insensitivity Syndrome Aneurysm Angina Pectoris Aniridia 1 Anorexia Nervosa 1 Anterior Segment Dysgenesis 4 Antisynthetase Syndrome Antithrombin Iii Deficiency Anuria Aortic Atherosclerosis Aphasia Aplasia of Lacrimal and Salivary Glands Aplastic Anemia Apolipoprotein C-Iii Deficiency Arthritis Arthrochalasia Ehlers-Danlos Syndrome Arthrogryposis, Renal Dysfunction, and Cholestasis 1 Arthropathy Aspergillosis Ataxia and Polyneuropathy, Adult-Onset Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus Atrial Fibrillation Atrioventricular Block Autoimmune Disease Autoimmune Hepatitis Autoimmune Inner Ear Disease Autoimmune Lymphoproliferative Syndrome, Type V Autoinflammation with Infantile Enterocolitis Autonomic Dysfunction Autonomic Neuropathy Autosomal Dominant Polycystic Kidney Disease Basal Cell Carcinoma B-Cell Lymphomas Bladder Urothelial Carcinoma Blastomycosis Bleeding Disorder, Platelet-Type, 11 Blepharochalasis 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 Brain Injury Broken Heart Syndrome Bronchiectasis Bronchopneumonia Brucellosis Budd-Chiari Syndrome Bullous Pemphigoid Calcinosis Camptocormism Cardiac Arrest Cardiac Arrhythmia Cardiac Sarcoidosis Cardiogenic Shock Cardiomyopathy, Familial Hypertrophic, 1 Cardiovascular Syphilis Caroli Disease Carpal Tunnel Syndrome Castleman Disease Celiac Disease 1 Cellulitis Cerebellar Degeneration Cerebral Amyloid Angiopathy, App-Related Cerebral Amyloid Angiopathy, Cst3-Related Cerebral Amyloid Angiopathy, Itm2b-Related, 1 Cerebral Hemorrhage Cerebritis Ceroid Lipofuscinosis, Neuronal, 5 Cervicitis Charcot-Marie-Tooth Disease Chediak-Higashi Syndrome Chitotriosidase Deficiency Cholangitis Cholestasis Cholestasis-Lymphedema Syndrome Choroiditis Chronic Graft Versus Host Disease Chronic Granulomatous Disease Chronic Myelomonocytic Leukemia Chronic Neutrophilic Leukemia Chronic Pyelonephritis Churg-Strauss Syndrome Chylomicron Retention Disease Cleft Larynx, Posterior Cohen-Gibson Syndrome Colchicine Resistance Colitis Collagen Disease Collagenous Colitis Colon Adenocarcinoma Colonic Pseudo-Obstruction Common Variable Immunodeficiency Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy Congenital Generalized Lipodystrophy Congestive Heart Failure Connective Tissue Disease Constrictive Pericarditis Corneal Dystrophy Corneal Dystrophy, Gelatinous Drop-Like Corneal Dystrophy, Lattice Type I Cranial Nerve Palsy Crescentic Glomerulonephritis Cryoglobulinemia Cryopyrin-Associated Periodic Syndrome Cutaneous T Cell Lymphoma Cutis Laxa Cystic Fibrosis Cystitis Delayed Sleep Phase Disorder Dementia Dense Deposit Disease Dermatitis Dermatomycosis Dermatomyositis Diabetes Insipidus Diabetes Mellitus Diarrhea Diastolic Heart Failure Diffuse Alveolar Hemorrhage Diffuse Large B-Cell Lymphoma Dilated Cardiomyopathy Discoid Lupus Erythematosus Disseminated Intravascular Coagulation Dominant Dystrophic Epidermolysis Bullosa Down Syndrome Duodenitis Early-Onset Familial Alzheimer Disease Ectropion Ehlers-Danlos Syndrome Encephalopathy Endocarditis Endotheliitis End Stage Renal Failure Enterocolitis Epiblepharon Epidermolysis Bullosa Epidermolysis Bullosa Acquisita Epidermolysis Bullosa Dystrophica, Autosomal Recessive Epithelioid Hemangioendothelioma Erdheim-Chester Disease Erysipeloid Evans' Syndrome Extramedullary Plasmacytoma Fabry Disease Facial Dysmorphism, Immunodeficiency, Livedo, and Short Stature Facial Paralysis Factor V Deficiency Factor X Deficiency Fainting Familial Adenomatous Polyposis 1 Familial Amyloidosis, Finnish Type Familial Cold Autoinflammatory Syndrome Familial Cold Autoinflammatory Syndrome 1 Familial Idiopathic Basal Ganglia Calcification Familial Lcat Deficiency Familial Mediterranean Fever Fanconi Anemia, Complementation Group E Fanconi Syndrome Femoral Neuropathy Filariasis Follicular Dendritic Cell Sarcoma Frontotemporal Dementia Gait Apraxia Gallbladder Cancer Gamma Heavy Chain Disease Ganglioneuroma Gastric Cancer Gastric Leiomyoma Gastric Lymphoma Gastritis Gastroduodenitis Gastrointestinal Lymphoma Gastrointestinal Stromal Tumor Gastrointestinal System Disease Gastrointestinal Tuberculosis Gingivitis Glanzmann Thrombasthenia Glomerulonephritis Glycogen Storage Disease Goiter Graft-Versus-Host Disease Granulocytopenia Haim-Munk Syndrome Hairy Cell Leukemia Hansen's Disease Hard Palate Cancer Headache Heavy Chain Deposition Disease Heavy Chain Disease Helicobacter Pylori Infection Hemangioendothelioma Hemarthrosis Hematopoietic Stem Cell Transplantation Hemorrhage, Intracerebral Hemosiderosis Hepatic Adenomas, Familial Hepatic Lipase Deficiency Hepatitis Hepatitis B Hepatitis C Hepatitis C Virus Hepatocellular Adenoma Hereditary Amyloidosis Hereditary Cerebral Amyloid Angiopathy Hereditary Neuropathies Hereditary Wilms' Tumor Hidradenitis Hidradenitis Suppurativa Hinman Syndrome Histiocytosis Hydrocele Hyperhidrosis, Gustatory Hyper-Igd Syndrome Hyperparathyroidism Hypersensitivity Vasculitis Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy Hypertensive Heart Disease Hyperthyroidism Hypertrophic Cardiomyopathy Hypoadrenalism Hypoaldosteronism Hypoalphalipoproteinemia, Primary Hypoglycemia Hypogonadism Hypoparathyroidism, Sensorineural Deafness, and Renal Disease Hypopituitarism Hyporeninemic Hypoaldosteronism Hypothyroidism, Thyroidal or Athyroidal, with Spiky Hair and Cleft Palate Ichthyosis Ichthyosis Vulgaris Idiopathic Recurrent Pericarditis Immune-Complex Glomerulonephritis Immunodeficiency 43 Immunoglobulin Alpha Deficiency Immunoglobulin E Concentration, Serum Immunotactoid Glomerulopathy Inclusion Body Myositis Incontinentia Pigmenti Infertility Inflammatory Bowel Disease Inflammatory Myopathy with Abundant Macrophages Insulin-Like Growth Factor I Intermittent Claudication Intermittent Hydrarthrosis Interstitial Cystitis Interstitial Keratitis Interstitial Nephritis Intestinal Pseudo-Obstruction Intrahepatic Cholestasis Invasive Aspergillosis Ischemic Colitis Ischemic Optic Neuropathy Juvenile Rheumatoid Arthritis Kaposiform Hemangioendothelioma Kartagener Syndrome Keratomalacia Keratopathy Keratosis Lacrimal Duct Defect Langerhans Cell Histiocytosis Laryngitis Laryngocele Lateral Sclerosis Lattice Corneal Dystrophy Lattice Corneal Dystrophy Type Ii Leiomyoma Leiomyosarcoma Lepromatous Leprosy Leukemia Lichen Amyloidosis Light and Heavy Chain Deposition Disease Light Chain Deposition Disease Lipodystrophy Lipoid Proteinosis of Urbach and Wiethe Lissencephaly 1 Liver Disease Lung Disease Lupus Erythematosus Lymphangioleiomyomatosis Lymphedema Lymphoblastic Leukemia Lymphoid Interstitial Pneumonia Lymphoma Lymphoma, Mucosa-Associated Lymphoid Type Lymphomatoid Papulosis Lymphoplasmacytic Lymphoma Lysosomal Storage Disease Macroglobulinemia Macroglossia Macular Amyloidosis Malaria Marden-Walker Syndrome Marginal Zone B-Cell Lymphoma Martsolf Syndrome Mediastinitis Medullary Sponge Kidney Megacolon Meibomian Cyst Membranoproliferative Glomerulonephritis Meningoencephalitis Mesangial Proliferative Glomerulonephritis Microscopic Polyangiitis Middle Lobe Syndrome Mixed Connective Tissue Disease Miyoshi Muscular Dystrophy 1 Mononeuropathy Mononeuropathy of the Median Nerve, Mild Morbid Obesity Motor Neuron Disease Mowat-Wilson Syndrome Muckle-Wells Syndrome Mucositis Multicentric Castleman Disease Multicentric Papillary Thyroid Carcinoma Multidrug-Resistant Tuberculosis Multifocal Motor Neuropathy Multiple Endocrine Neoplasia Multiple Endocrine Neoplasia, Type Iia Multiple Sclerosis Muscular Dystrophy Myasthenia Gravis Mycobacterium Chelonae Mycosis Fungoides Myd88 Deficiency Myelofibrosis Myeloma, Multiple Myocardial Infarction Myocarditis Myopathy Myositis Nasopharyngitis Necrobiotic Xanthogranuloma Nephrotic Syndrome Nephrotic Syndrome, Type 1 Neuroendocrine Tumor Neuroma Neuronitis Neuropathy Neurotrophic Keratopathy Niemann-Pick Disease Nodular Cutaneous Amyloidosis Nodular Nonsuppurative Panniculitis Nodular Regenerative Hyperplasia Non-Secretory Myeloma Notalgia Paresthetica Odontoma Oncocytoma Osteomyelitis Osteopoikilosis Ovarian Hyperstimulation Syndrome Pancreatic Neuroendocrine Tumor Pancreatitis Panniculitis Papillary Carcinoma Papular Mucinosis Paraganglioma Paraplegia Paronychia Pdgfrb-Associated Chronic Eosinophilic Leukemia Pellagra Pellucid Marginal Degeneration Pericardial Effusion Pericarditis Periodic Fever, Familial, Autosomal Dominant Periodontal Disease Periodontitis Peritonitis Pharyngitis Pheochromocytoma Pick Disease of Brain Pigmentary Disorder, Reticulate, with Systemic Manifestations, X-Linked Pituitary Adenoma Plasma Cell Leukemia Plasmacytoma Pneumatosis Cystoides Intestinalis Pneumonia Poems Syndrome Polyarteritis Nodosa Polycystic Kidney Disease Polyneuropathy Porokeratosis Porokeratosis 1, Multiple Types Porphyria Portal Hypertension Postural Hypotension Premature Ovarian Failure 1 Premature Ovarian Failure 7 Presbyopia Primary Agammaglobulinemia Primary Biliary Cirrhosis Primary Cutaneous Amyloidosis Primary Hyperparathyroidism Primary Localized Amyloidosis Progressive Multifocal Leukoencephalopathy Proliferative Glomerulonephritis Prostatitis Prosthetic Joint Infection Protein-Losing Enteropathy Prurigo Nodularis Pseudoxanthoma Elasticum Psoriasis Psoriasis 13 Psoriatic Arthritis Psoriatic Juvenile Idiopathic Arthritis Pulmonary Alveolar Proteinosis Pulmonary Hemosiderosis Pulmonary Hypertension Pulmonary Sarcoidosis Pure Red-Cell Aplasia Purpura Pyelonephritis Pyloric Stenosis Rapidly Progressive Glomerulonephritis Reactive Arthritis Recessive Dystrophic Epidermolysis Bullosa Relapsing Polychondritis Renal Oncocytoma Restrictive Cardiomyopathy Reticulosarcoma Retinitis Retinitis Pigmentosa Retinitis Pigmentosa 7 Retroperitoneal Fibrosis Rheumatic Disease Rheumatoid Arthritis Ring Dermoid of Cornea Rosai-Dorfman Disease Salt and Pepper Developmental Regression Syndrome Sapho Syndrome Sarcoidosis 2 Sarcoma Scabies Schnitzler Syndrome Scleredema Sclerosing Cholangitis Scoliosis, Isolated 1 Scott Syndrome Senile Plaque Formation Sensorineural Hearing Loss Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis Sickle Cell Anemia Sick Sinus Syndrome Siderosis Sinusitis Sjogren Syndrome Skeletal Tuberculosis Skin Sarcoidosis Smoldering Myeloma Solitary Osseous Plasmacytoma Spasticity Spinal Cord Injury Splenic Infarction Spondylarthropathy Spondylitis Spondyloarthropathy Spondyloarthropathy 1 Spondylocarpotarsal Synostosis Syndrome Steatorrhea Subacute Thyroiditis Superficial Siderosis Suppurative Cholangitis Sveinsson Chorioretinal Atrophy Syncope Synucleinopathy Syphilis Systemic Lupus Erythematosus Systemic Mastocytosis Systemic Onset Juvenile Idiopathic Arthritis T-Cell Leukemia Temporal Arteritis Tertiary Syphilis Thrombasthenia Thrombosis Thymoma Thyroid Cancer Thyroiditis Tonsillitis Tooth Disease Toxic Megacolon Tracheobronchomalacia Tracheobronchomegaly Tracheobronchopathia Osteoplastica Tracheomalacia Transitional Cell Carcinoma Treacher Collins Syndrome 1 Tuberculoid Leprosy Ulcerative Colitis Undifferentiated Pleomorphic Sarcoma Uremia Ureteral Obstruction Urinary Tract Obstruction Urticaria Urticaria Pigmentosa Vascular Dementia Vasculitis Vulvar Intraepithelial Neoplasia Waldenstrom Macroglobulinemia Wells Syndrome Whipple Disease Wild Type Abeta2m Amyloidosis Wild Type Attr Amyloidosis Xanthogranulomatous Pyelonephritis