Informaţii despre

Nume Myositis
Pagina Web www.malacards.org
Clasificare globală Malacards Boli genetice; Boli infecțioase; Boli rare
Clasificari ICD10 Myositis in other infectious diseases classified elsewhere; Myositis, unspecified
Clasificare anatomică Malacards Boli musculare; Boli neuronale
Boli din aceeaşi familie Bacterial Myositis; Viral Myositis

Vezi şi

Boli A-Z Aarskog-Scott Syndrome Abducens Nerve Disease Acquired Immunodeficiency Syndrome Acute Respiratory Distress Syndrome Adenocarcinoma Adult Dermatomyositis Agammaglobulinemia Aging Aland Island Eye Disease Alopecia Alopecia, Neurologic Defects, and Endocrinopathy Syndrome Alopecia Totalis Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity Alport Syndrome, X-Linked Al-Raqad Syndrome Alveolar Soft Part Sarcoma Alzheimer Disease Alzheimer Disease 3 Amyloidosis Anaplastic Large Cell Lymphoma Anauxetic Dysplasia 1 Androgen Insensitivity, Partial Androgen Insensitivity Syndrome, Mild Aneurysm Aneurysmal Bone Cysts Angioimmunoblastic Lymphadenopathy with Dysproteinemia Angiomatosis Aniridia 1 Ankylosis Annular Erythema Anorexia Nervosa 1 Anterior Compartment Syndrome Anterior Segment Dysgenesis 4 Anterior Uveitis Antiphospholipid Syndrome Antisynthetase Syndrome Aphthous Stomatitis Aplastic Anemia Appendicitis Arthritis Arthrochalasia Ehlers-Danlos Syndrome Arthrogryposis, Renal Dysfunction, and Cholestasis 1 Arthropathy Atrioventricular Block Autoimmune Disease Autoimmune Lymphoproliferative Syndrome Autoimmune Lymphoproliferative Syndrome, Type V Autosomal Recessive Limb-Girdle Muscular Dystrophy Autosomal Recessive Limb-Girdle Muscular Dystrophy Type 2b Autosomal Recessive Limb-Girdle Muscular Dystrophy Type 2f Autosomal Recessive Limb-Girdle Muscular Dystrophy Type 2h Axonal Neuropathy Bacillary Angiomatosis Back Pain Bacterial Myositis B-Cell Lymphomas Bethlem Myopathy 1 Bleeding Disorder, Platelet-Type, 11 Blood Group--Ahonen Blood Group, Dombrock System Blood Group, I System Breast Cancer Breast Rhabdomyosarcoma Brucellosis Bursitis Calcinosis Camptocormism Candidiasis Cardioneuromyopathy with Hyaline Masses and Nemaline Rods Cellulitis Central Nervous System Disease Cerebral Amyloid Angiopathy, Cst3-Related Cerebral Palsy Cerebritis Cervicitis Cherubism Chickenpox Chikungunya Childhood Leukemia Childhood Type Dermatomyositis Cholangitis Chondrosarcoma Chorioretinitis Chromosome 16p13.3 Deletion Syndrome, Proximal Chromosome Xp21 Deletion Syndrome Chronic Active Epstein-Barr Virus Infection Chronic Graft Versus Host Disease Chronic Mucocutaneous Candidiasis Churg-Strauss Syndrome Clear Cell Chondrosarcoma Coffin-Siris Syndrome 1 Colitis Collagen Disease Common Variable Immunodeficiency Compartment Syndrome Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy Congenital Radioulnar Synostosis Congenital Toxoplasmosis Connective Tissue Disease Constrictive Pericarditis Craniofacial Dysmorphism, Skeletal Anomalies, and Mental Retardation Syndrome Creatine Phosphokinase, Elevated Serum Crescentic Glomerulonephritis Creutzfeldt-Jakob Disease Crohn's Colitis Crohn's Disease Cryptogenic Organizing Pneumonia Cutaneous Lupus Erythematosus Cutaneous Sclerosis Dacryoadenitis Dengue Virus Dermatitis Dermatomyositis Diabetes Mellitus Dilated Cardiomyopathy Discoid Lupus Erythematosus Distal Muscular Dystrophy Duodenitis Duodenum Cancer Dyskinesia of Esophagus Dysphagia Emery-Dreifuss Muscular Dystrophy Encephalitis Encephalopathy Endocarditis Endometrial Cancer Endotheliitis Eosinophilic Fasciitis Eosinophilic Granulomatosis with Polyangiitis Epithelial Recurrent Erosion Dystrophy Erythema Infectiosum Ewing Sarcoma Exophthalmos Extrapulmonary Tuberculosis Factor Xi Deficiency Familial Mediterranean Fever Fasciitis Fibrodysplasia Ossificans Progressiva Fibroosseous Pseudotumor of Digits Fibrous Dysplasia Focal Myositis Fungal Myositis Gas Gangrene Gastritis Giant Cell Myocarditis Glomerulonephritis Glycogen Storage Disease V Graft-Versus-Host Disease Granulomatous Myositis Graves' Disease Griscelli Syndrome Griscelli Syndrome, Type 2 Haemophilus Influenzae Hansen's Disease Hantavirus Pulmonary Syndrome Helicobacter Pylori Infection Hemolytic Anemia Hemophilia Hepatic Adenomas, Familial Hepatitis Hepatitis B Hepatitis C Hepatitis C Virus Hepatitis E Hepatocellular Carcinoma Herpes Zoster Herpes Zoster Ophthalmicus Histoplasmosis Human Coronavirus Sensitivity Human Immunodeficiency Virus Type 1 Hypereosinophilic Syndrome Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy Hypertrophic Cardiomyopathy Hypertrophic Osteoarthropathy, Primary, Autosomal Recessive, 1 Hypokalemia Hypoparathyroidism Idiopathic Eosinophilic Myositis Idiopathic Inflammatory Myopathy Immune-Complex Glomerulonephritis Inclusion Body Myositis Indian Tick Typhus Infective Myositis Inflammatory Bowel Disease 1 Influenza Insulin-Like Growth Factor I Interstitial Lung Disease Interstitial Myocarditis Intestinal Pseudo-Obstruction Ischemia Isolated Hyperckemia Jackhammer Esophagus Juvenile Overlap Myositis Lactic Acidosis Lagophthalmos Laryngitis Lateral Sclerosis Lepromatous Leprosy Leukemia Limb-Girdle Muscular Dystrophy Linear Scleroderma Lipodystrophy Localized Lipodystrophy Lung Cancer Lung Disease Lupus Erythematosus Lyme Disease Lymphoma Macroglossia Macrophagic Myofasciitis Major Affective Disorder 2 Mal De Meleda Malignant Hyperthermia Malignant Mesenchymoma Malignant Triton Tumor Mannose-Binding Lectin Deficiency Melanoma Melanotic Neurilemmoma Membranoproliferative Glomerulonephritis Meningoencephalitis Mental Retardation-Hypotonic Facies Syndrome, X-Linked, 1 Mesenchymoma Metabolic Encephalomyopathic Crises, Recurrent, with Rhabdomyolysis, Cardiac Arrhythmias, and Neurodegeneration Microscopic Polyangiitis Microsporidiosis Mixed Connective Tissue Disease Mixed-Type Autoimmune Hemolytic Anemia Miyoshi Muscular Dystrophy 1 Mononeuropathy Motor Neuron Disease Mucopolysaccharidosis, Type Vii Multicentric Reticulohistiocytosis Multiple System Atrophy 1 Mumps Muscle Disorders Muscle Hypertrophy Muscle Tissue Disease Muscular Atrophy Muscular Dystrophy Muscular Dystrophy, Duchenne Type Muscular Dystrophy-Dystroglycanopathy , Type C, 5 Muscular Dystrophy, Limb-Girdle, Type 1c Muscular Dystrophy, Limb-Girdle, Type 2a Muscular Dystrophy, Limb-Girdle, Type 2b Muscular Dystrophy, Limb-Girdle, Type 2c Muscular Dystrophy, Limb-Girdle, Type 2d Muscular Dystrophy, Limb-Girdle, Type 2f Muscular Dystrophy, Limb-Girdle, Type 2g Muscular Dystrophy, Limb-Girdle, Type 2h Muscular Dystrophy, Limb-Girdle, Type 2j Myasthenia Gravis Myelitis Myelodysplastic Syndrome Myeloid Leukemia Myeloproliferative Neoplasm Myocarditis Myofibrillar Myopathy Myopathy Myositis Fibrosa Myositis Ossificans Myotonia Myotonia Congenita Nasopharyngeal Carcinoma Nasopharyngitis Necrotizing Autoimmune Myopathy Necrotizing Fasciitis Neuroleptic Malignant Syndrome Neuromuscular Disease Neuronitis Neuronopathy, Distal Hereditary Motor, Type Viib Neuropathy Niemann-Pick Disease Niemann-Pick Disease, Type B Nocardiosis Occipital Horn Syndrome Oculopharyngeal Muscular Dystrophy Oral Submucous Fibrosis Orbital Cellulitis Orbital Plasma Cell Granuloma Orchitis Osseous Heteroplasia, Progressive Osteogenic Sarcoma Osteoid Osteoma Osteomalacia Osteomyelitis Overhydrated Hereditary Stomatocytosis Overlap Myositis Pancreatic Cancer Pancreatitis Pancytopenia Panniculitis Paraneoplastic Syndromes Parkinson Disease 15, Autosomal Recessive Early-Onset Pediatric Systemic Lupus Erythematosus Pericardial Effusion Pericarditis Perimyositis Periostitis Peripheral T-Cell Lymphoma Phaeochromocytoma Pharyngitis Pheochromocytoma Pick Disease of Brain Piriformis Syndrome Pleomorphic Rhabdomyosarcoma Plexopathy Pneumonia Poliomyelitis Polyarteritis Nodosa Polydactyly, Postaxial, with Progressive Myopia Polyglucosan Body Myopathy 1 with or Without Immunodeficiency Polymyositis Polyneuropathy Posterior Myocardial Infarction Posterior Scleritis Primary Biliary Cirrhosis Proliferative Fasciitis Proteus Syndrome Pseudohypoparathyroidism Psoriatic Arthritis Ptosis Pulmonary Fibrosis Pulmonary Fibrosis and/or Bone Marrow Failure, Telomere-Related, 2 Pulmonary Sarcoidosis Purpura Pyoderma Pyoderma Gangrenosum Pyomyositis Quadriplegia Radiculopathy Radioulnar Synostosis Reducing Body Myopathy Refsum Disease, Classic Relapsing Polychondritis Rhabdomyosarcoma Rheumatic Disease Rheumatic Heart Disease Rheumatoid Arthritis Rheumatoid Vasculitis Rigid Spine Muscular Dystrophy 1 Salt and Pepper Developmental Regression Syndrome Sarcoidosis 2 Sarcoma Sarcosporidioză Scleredema Scleredema Adultorum Scleritis Scleromyxedema Secondary Syphilis Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis Sialadenitis Sleep Disorder Soft Tissue Sarcoma Sparganosis Spasticity Spastic Paraparesis Spinal and Bulbar Muscular Atrophy, X-Linked 1 Spinal Cord Injury Spindle Cell Lipoma Spindle Cell Rhabdomyosarcoma Spondylitis Spondyloarthropathy 1 Spondyloocular Syndrome Squamous Cell Carcinoma Strabismus Streptococcal Group a Invasive Disease Streptococcal Toxic-Shock Syndrome Subacute Cutaneous Lupus Erythematosus Sveinsson Chorioretinal Atrophy Synostosis Synovitis Syphilis Systemic Lupus Erythematosus Systemic Onset Juvenile Idiopathic Arthritis Takenouchi-Kosaki Syndrome T-Cell Leukemia Tenosynovitis Tetanus Tetrasomy 9p Third-Degree Atrioventricular Block Thrombocytopenia Thrombophlebitis Thrombosis Thymic Hyperplasia Thymoma Thyroiditis Tick-Borne Encephalitis Toxic Shock Syndrome Toxoplasmoză Transitional Cell Carcinoma Transverse Myelitis Treacher Collins Syndrome 1 Tremor Trichinosis Trochleitis Ulcerative Colitis Undifferentiated Connective Tissue Disease Uveitis Vaginitis Vasculitis Viral Myositis Virus Associated Hemophagocytic Syndrome Vitamin B12 Deficiency Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 6 Welander Distal Myopathy Welander Distal Myopathy, Swedish Type West Nile Virus Yao Syndrome