Informaţii despre

Nume Scleroderma, Familial Progressive
Pagina Web www.malacards.org
Clasificare globală Malacards Boli genetice; Boli rare
Clasificari ICD10 CR(E)ST syndrome; Other forms of systemic sclerosis; Progressive systemic sclerosis; Systemic sclerosis induced by drugs and chemicals; Systemic sclerosis, unspecified
Clasificare anatomică Malacards Boli ale sistemului imunitar; Boli de piele; Boli nefrologice (ale rinichilor); Boli neuronale; Boli osoase; Boli respiratorii
Boli din aceeaşi familie Localized Scleroderma

Vezi şi

Boli A-Z Acalculous Cholecystitis Achalasia Acrocallosal Syndrome Acroosteolysis Actinomycosis Acute Interstitial Pneumonia Acute Leukemia of Ambiguous Lineage Acute Myocardial Infarction Acute Myocarditis Aging Al Kaissi Syndrome Alopecia, Neurologic Defects, and Endocrinopathy Syndrome Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity Alpha-Fetoprotein Deficiency Alport Syndrome, X-Linked Al-Raqad Syndrome Amyloidosis Anca-Associated Vasculitis Angioimmunoblastic T-Cell Lymphoma Angiosarcoma Aniridia 1 Anorexia Nervosa 1 Antiphospholipid Syndrome Antisynthetase Syndrome Aortic Coarctation Aplastic Anemia Arthritis Arthrochalasia Ehlers-Danlos Syndrome Arthropathy Ataxia and Polyneuropathy, Adult-Onset Atlantoaxial Subluxation Autoimmune Disease Autoimmune Hepatitis Autoimmune Inner Ear Disease Autoimmune Myocarditis Autonomic Dysfunction Blastoma Bleeding Disorder, Platelet-Type, 11 Blood Group--Ahonen Blood Group, Dombrock System Blood Group, I System Blue Toe Syndrome Breast Cancer Brittle Bone Disorder Bronchiolitis Bronchiolitis Obliterans Bruck Syndrome Bullous Pemphigoid Bursitis Caffey Disease Calcinosis Candidiasis Capillary Hemangioma Capillary Leak Syndrome Cardiac Tamponade Central Cord Syndrome Central Nervous System Vasculitis Cerebritis Cervicitis Cholecystitis Cholecystolithiasis Chronic Graft Versus Host Disease Cold Agglutinin Disease Colitis Collagen Disease Collagenous Colitis Common Variable Immunodeficiency Congestive Heart Failure Connective Tissue Disease Coronary Stenosis Crescentic Glomerulonephritis Crest Syndrome Critical Limb Ischemia Cryoglobulinemia Cryoglobulinemia, Familial Mixed Cutaneous Polyarteritis Nodosa Cytochrome P450 2d6 Variant Cytomegalovirus Infection Dentinogenesis Imperfecta Dermatitis Dermatofibrosarcoma Protuberans Dermatomyositis Desquamative Interstitial Pneumonia Diabetes Mellitus Diffuse Alveolar Hemorrhage Diffuse Cutaneous Systemic Sclerosis Diffuse Idiopathic Skeletal Hyperostosis Diffuse Scleroderma Discoid Lupus Erythematosus Duodenitis Ehlers-Danlos/osteogenesis Imperfecta Syndrome Ehlers-Danlos Syndrome Ehlers-Danlos Syndrome, Arthrochalasia Type, 1 Ehlers-Danlos Syndrome, Classic Type, 1 Elastosis Perforans Serpiginosa Elephantiasis Encephalopathy Endocarditis Endotheliitis Enthesopathy Eosinophilic Fasciitis Epidermolytic Hyperkeratosis Epithelial Recurrent Erosion Dystrophy Esophageal Candidiasis Esophageal Disease Euthyroid Sick Syndrome Extragonadal Seminoma Factor X Deficiency Fanconi Anemia, Complementation Group E Fanconi Syndrome Fasciitis Fecal Incontinence Gastric Antral Vascular Ectasia Gastroesophageal Reflux Gingival Fibromatosis Gingival Overgrowth Gingivitis Glomerulonephritis Graft-Versus-Host Disease Granulomatous Dermatitis Graves' Disease Hansen's Disease Headache Hemangioma Hemangioma-Thrombocytopenia Syndrome Hematopoietic Stem Cell Transplantation Hemiplegia Hemolytic Anemia Hemolytic-Uremic Syndrome Hepatic Adenomas, Familial Hepatitis Hepatitis a Hepatitis C Hepatitis C Virus High Bone Mass Osteogenesis Imperfecta Histiocytosis Hyperaldosteronism, Familial, Type I Hyperostosis Hyperprolactinemia Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy Hypertrophic Scars Hypoglycemia Hypogonadotropic Hypogonadism 1 with or Without Anosmia Hypoparathyroidism Hypopituitarism Hypoxia Idiopathic Interstitial Pneumonia Idiopathic Scoliosis Immune Defect Due to Absence of Thymus Immunoglobulin E Concentration, Serum Impotence Inclusion Body Myositis Infective Endocarditis Inferior Myocardial Infarction Inner Ear Disease Interstitial Lung Disease Intestinal Disease Intestinal Perforation Intestinal Pseudo-Obstruction Intracranial Hypotension Ischemia Juvenile Temporal Arteritis Kabuki Syndrome 1 Keloids Langerhans Cell Histiocytosis Larsen-Like Syndrome Lathyrism Lepromatous Leprosy Leukemia Lichen Sclerosus Limb Ischemia Limited Scleroderma Linear Scleroderma Lipodermatosclerosis Lipomatosis, Multiple Liver Cirrhosis Localized Scleroderma Lung Disease Lupus Erythematosus Lymphangiectasia, Intestinal Lymphoma Lymphoma, Mucosa-Associated Lymphoid Type Lymphopenia Malignant Hypertension Malignant Pleural Mesothelioma Marfan Syndrome Mediastinitis Megacolon Megaesophagus Microscopic Polyangiitis Mixed Connective Tissue Disease Mononeuropathy Mucopolysaccharidosis, Type Vii Multicentric Reticulohistiocytosis Multiple Mitochondrial Dysfunctions Syndrome 5 Multiple Sclerosis Mycosis Fungoides Myelitis Myelofibrosis Myocardial Infarction Myocarditis Myopathy Myositis Nasopharyngeal Carcinoma Nasopharyngitis Necrotizing Fasciitis Neonatal Scleroderma Nephrogenic Systemic Fibrosis Nephrotic Syndrome Neuritis Neuromyelitis Optica Neuromyelitis Optica Spectrum Disorder Neuronitis Neuropathy Neutrophil Actin Dysfunction Nodular Regenerative Hyperplasia Nonspecific Interstitial Pneumonia Nontuberculous Mycobacterial Lung Disease Ocular Albinism Optic Neuritis Osteoarthritis Osteoarthritis with Mild Chondrodysplasia Osteogenesis Imperfecta, Type I Osteogenesis Imperfecta, Type Ii Osteogenesis Imperfecta, Type Iii Osteogenesis Imperfecta, Type Iv Osteogenesis Imperfecta, Type V Osteogenesis Imperfecta, Type Vi Osteogenesis Imperfecta, Type Vii Osteogenesis Imperfecta, Type Viii Osteomalacia Osteomyelitis Osteonecrosis Overlap Myositis Panniculitis Papular Mucinosis Paramyotonia Congenita of Von Eulenburg Parotitis Pericardial Effusion Pericarditis Pernicious Anemia Pityriasis Rubra Pilaris Pneumatosis Cystoides Intestinalis Pneumoconiosis Pneumonia Pneumothorax Poems Syndrome Polyarteritis Nodosa Polydactyly, Postaxial, with Progressive Myopia Polymyositis Porphyria Porphyria Cutanea Tarda Potocki-Shaffer Syndrome Primary Biliary Cirrhosis Primary Hypertrophic Osteoarthropathy Pseudoainhum Pseudoxanthoma Elasticum Psoriasis Psoriasis 13 Psoriatic Arthritis Pulmonary Alveolar Proteinosis Pulmonary Blastoma Pulmonary Fibrosis Pulmonary Fibrosis and/or Bone Marrow Failure, Telomere-Related, 2 Pulmonary Fibrosis, Idiopathic Pulmonary Hypertension Pulmonary Sarcoidosis Pulmonary Systemic Sclerosis Pure Red-Cell Aplasia Purpura Pyoderma Pyoderma Gangrenosum Pyomyositis Rapidly Progressive Glomerulonephritis Raynaud Disease Refractory Anemia Renal Fibrosis Restless Legs Syndrome Retinal Artery Occlusion Retinal Vasculitis Retinitis Retroperitoneal Fibrosis Reynolds Syndrome Rheumatic Disease Rheumatoid Arthritis Right Bundle Branch Block Sarcoidosis 2 Scabies Scoliosis Seminoma Sickle Cell Disease Siderosis Silicosis Skin Disease Small Cell Carcinoma Spinal Stenosis Spondylitis Spondyloarthropathy 1 Spondyloocular Syndrome Spontaneous Intracranial Hypotension Steatorrhea Stiff Skin Syndrome Superficial Siderosis Superficial Siderosis of the Central Nervous System Systemic Lupus Erythematosus Systemic Scleroderma Telangiectasis Temporal Arteritis Testicular Regression Syndrome Thoracic Outlet Syndrome Thrombocytopenia Thrombocytosis Thrombotic Thrombocytopenic Purpura Thyroid Cancer Thyroiditis Toxic Oil Syndrome Transverse Myelitis Trigeminal Neuralgia Ulnar Neuropathy Undifferentiated Connective Tissue Disease Vascular Disease Vasculitis Viral Hepatitis Visceral Myopathy Vitamin B12 Deficiency Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 6 Wernicke Encephalopathy Wolff-Parkinson-White Syndrome