Informaţii despre

Nume Al Amyloidosis
Pagina Web www.malacards.org
Clasificare globală Malacards Boli genetice; Boli metabolice; Boli rare
Clasificari ICD10 Amyloidosis, unspecified; Non-neuropathic heredofamilial amyloidosis
Clasificare anatomică Malacards Boli ale sistemului imunitar; Boli de sânge; Boli nefrologice (ale rinichilor); Boli neuronale; Boli osoase
Boli din aceeaşi familie Ah Amyloidosis; Amyloidosis Aa; Hereditary Amyloidosis; Primary Localized Amyloidosis

Vezi şi

Boli A-Z 3-Hydroxyacyl-Coa Dehydrogenase Deficiency Aarskog-Scott Syndrome Acquired Von Willebrand Syndrome Acute Liver Failure Acute Respiratory Distress Syndrome Adenocarcinoma Adult T-Cell Leukemia Aging Ah Amyloidosis Alopecia, Neurologic Defects, and Endocrinopathy Syndrome Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity Alport Syndrome, X-Linked Al-Raqad Syndrome Amyloidosis Amyloidosis Aa Amyloidosis, Familial Visceral Amyloidosis, Finnish Type Amyloid Tumor Amyotrophic Lateral Sclerosis 1 Aniridia 1 Anorexia Nervosa 1 Anterior Segment Dysgenesis 4 Arthritis Arthrochalasia Ehlers-Danlos Syndrome Atrial Fibrillation Autoimmune Disease Autoimmune Lymphoproliferative Syndrome, Type V Autonomic Neuropathy B-Cell Lymphomas Bleeding Disorder, Platelet-Type, 11 Blood Group--Ahonen Blood Group, Dombrock System Blood Group, I System Budd-Chiari Syndrome Cardiogenic Shock Cardiomyopathy, Familial Hypertrophic, 1 Cholangitis Cholestasis Chronic Ulcer of Skin Cleft Larynx, Posterior Cohen-Gibson Syndrome Colitis Collagenous Colitis Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy Congestive Heart Failure Cranial Nerve Palsy Diabetes Insipidus Diarrhea Diffuse Large B-Cell Lymphoma Dilated Cardiomyopathy Disseminated Intravascular Coagulation Endotheliitis Essential Thrombocythemia Factor V Deficiency Factor X Deficiency Gastric Cancer Gastroduodenitis Glomerulonephritis Goiter Hairy Cell Leukemia Hematopoietic Stem Cell Transplantation Hepatic Adenomas, Familial Hepatitis Hepatitis C Hepatitis C Virus Hereditary Amyloidosis Hinman Syndrome Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy Hypoglycemia Intrahepatic Cholestasis Keratomalacia Laryngitis Leukemia Light Chain Deposition Disease Liver Disease Lung Disease Lymphangiosarcoma Lymphoblastic Leukemia Lymphoma Macroglobulinemia Macroglossia Martsolf Syndrome Mediastinitis Megacolon Miyoshi Muscular Dystrophy 1 Motor Neuron Disease Mucositis Myeloma, Multiple Myopathy Nephrotic Syndrome Neuronitis Neuropathy Niemann-Pick Disease Pancreatitis Peritonitis Pick Disease of Brain Plasmacytoma Poems Syndrome Polyneuropathy Primary Localized Amyloidosis Prostatitis Pulmonary Hypertension Rapidly Progressive Glomerulonephritis Retinitis Pigmentosa 7 Rheumatoid Arthritis Ring Dermoid of Cornea Scleredema Scott Syndrome Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis Spondylocarpotarsal Synostosis Syndrome Suppurative Cholangitis Sveinsson Chorioretinal Atrophy T-Cell Leukemia Temporal Arteritis Thrombosis Thyroiditis Tonsillitis Toxic Megacolon Treacher Collins Syndrome 1 Ulcerative Colitis Undifferentiated Pleomorphic Sarcoma Varicose Veins Venous Insufficiency