Informaţii despre

Nume Myopathy
Pagina Web www.malacards.org
Clasificare globală Malacards Boli rare
Clasificari ICD10 Disorder of muscle, unspecified; Myopathy, unspecified
Clasificare anatomică Malacards Boli musculare
Boli din aceeaşi familie Benign Autosomal Dominant Myopathy; Gne-Related Myopathy; Myopathy Due to Malate-Aspartate Shuttle Defect; Myopathy, Congenital

Vezi şi

Boli A-Z Aarskog-Scott Syndrome Abetalipoproteinemia Acromegaly Acromesomelic Dysplasia Acute Graft Versus Host Disease Acute Hemorrhagic Leukoencephalitis Acute Liver Failure Acute Myocardial Infarction Acute Myocarditis Acute Respiratory Distress Syndrome Acyl-Coa Dehydrogenase, Short-Chain, Deficiency of Acyl-Coa Dehydrogenase, Very Long-Chain, Deficiency of Adenocarcinoma Adenoma Adrenal Adenoma Adult-Onset Nemaline Myopathy Aging Al Amyloidosis Alcoholic Cardiomyopathy Alexia Al-Gazali-Bakalinova Syndrome Alopecia 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 Aminoaciduria Amyloid Neuropathy Amyloidosis Amyotonia Congenita Amyotrophic Lateral Sclerosis 1 Andersen Cardiodysrhythmic Periodic Paralysis Androgenic Alopecia Aniridia 1 Ankylosis Anorexia Nervosa 1 Anterior Compartment Syndrome Anterograde Amnesia Antisynthetase Syndrome Appendicitis Arrhythmogenic Right Ventricular Cardiomyopathy Arthritis Arthrochalasia Ehlers-Danlos Syndrome Arthrogryposis, Distal, Type 9 Arthrogryposis Multiplex Congenita, Neurogenic, with Myelin Defect Arthropathy Asphyxia Neonatorum Aspiration Pneumonia Ataxia and Polyneuropathy, Adult-Onset Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus Ataxia-Oculomotor Apraxia 3 Atrial Fibrillation Atrial Standstill Atrial Standstill 1 Atrioventricular Block Autism Autonomic Dysfunction Autosomal Dominant Limb-Girdle Muscular Dystrophy Autosomal Dominant Limb-Girdle Muscular Dystrophy Type 1c Autosomal Dominant Optic Atrophy Plus Syndrome Autosomal Dominant Progressive External Ophthalmoplegia Autosomal Recessive Limb-Girdle Muscular Dystrophy Autosomal Recessive Limb-Girdle Muscular Dystrophy Type 2b Autosomal Recessive Limb-Girdle Muscular Dystrophy Type 2e Autosomal Recessive Limb-Girdle Muscular Dystrophy Type 2f Autosomal Recessive Limb-Girdle Muscular Dystrophy Type 2h Axonal Neuropathy Ayme-Gripp Syndrome Bannayan-Riley-Ruvalcaba Syndrome Barth Syndrome B-Cell Lymphomas Behr Syndrome Benign Autosomal Dominant Myopathy Beriberi Beta-Thalassemia Bethlem Myopathy 1 Biotinidase Deficiency Bleeding Disorder, Platelet-Type, 11 Blepharophimosis 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 Bornholm Eye Disease Branchiootic Syndrome 1 Breast Rhabdomyosarcoma Brody Myopathy Bronchiolitis Bronchiolitis Obliterans Bursitis Calcinosis Calciphylaxis Camptocormism Candidiasis Cap Myopathy Cardiac Arrest Cardiac Arrhythmia Cardiac Conduction Defect Cardiac Tamponade Cardiogenic Shock Cardiomyopathy, Dilated, 1a Cardiomyopathy, Dilated, 1b Cardiomyopathy, Dilated, 3b Cardioneuromyopathy with Hyaline Masses and Nemaline Rods Carey-Fineman-Ziter Syndrome Carotid Artery Occlusion Cataract Cataract 5, Multiple Types Central Core Disease of Muscle Central Core Myopathy Centronuclear Myopathy Cerebellar Hypoplasia Cerebritis Cerebrotendinous Xanthomatosis Cervicitis Charcot-Marie-Tooth Disease Charcot-Marie-Tooth Disease, Dominant Intermediate B Chikungunya Childhood-Onset Nemaline Myopathy Cholangiocarcinoma Cholestasis Chorea, Childhood-Onset, with Psychomotor Retardation Choreatic Disease Choroiditis Chromosome 1p36 Deletion Syndrome Chromosome Xp21 Deletion Syndrome Chronic Fatigue Syndrome Chronic Graft Versus Host Disease Chronic Inflammatory Demyelinating Polyneuropathy Chronic Intestinal Pseudoobstruction Chronic Progressive External Ophthalmoplegia Cleidocranial Dysplasia Clubfoot Collagen Vi-Related Myopathy Common Variable Immunodeficiency Communicating Hydrocephalus Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy Congenital Contractures Congenital Disorder of Glycosylation, Type Iid Congenital Fiber-Type Disproportion Congenital Generalized Lipodystrophy Congenital Myasthenic Syndrome Congenital Nonspherocytic Hemolytic Anemia Congenital Ptosis Congenital Structural Myopathy Congestive Heart Failure Connective Tissue Disease Constipation Craniosynostosis Creatine Deficiency Syndromes Creatine Phosphokinase, Elevated Serum Critical Illness Polyneuropathy Cutaneous Sclerosis Cutis Laxa Cystinosis Cytophagic Histiocytic Panniculitis Cytoplasmic Body Myopathy Danon Disease Dementia Demyelinating Polyneuropathy Deoxyguanosine Kinase Deficiency Dermatitis Dermatitis Herpetiformis Dermatomyositis Diabetes Mellitus Diarrhea Dihydrolipoamide Dehydrogenase Deficiency Dilated Cardiomyopathy Distal Arthrogryposis Distal Hereditary Motor Neuropathies Distal Muscular Dystrophy Distal Myopathy with Vocal Cord Weakness Dysautonomia Dysferlinopathy Dyskeratosis Congenita Dysphagia Dystrophinopathies Ectodermal Dysplasia Ehlers-Danlos Syndrome Ehlers-Danlos Syndrome, Classic-Like Ehlers-Danlos Syndrome, Kyphoscoliotic Type, 2 Emery-Dreifuss Muscular Dystrophy Emery-Dreifuss Muscular Dystrophy 2, Autosomal Dominant Emery-Dreifuss Muscular Dystrophy, X-Linked Encephalomyopathy Encephalopathy Endocardial Fibroelastosis Endomyocardial Fibrosis Endotheliitis Eosinophilia-Myalgia Syndrome Eosinophilic Fasciitis Eosinophilic Pneumonia Epidermolysis Bullosa Epidermolysis Bullosa Simplex Epilepsy Epithelial Recurrent Erosion Dystrophy Erythromelalgia Exophthalmic Ophthalmoplegia Exophthalmos Extracardiac Rhabdomyoma Extrapulmonary Tuberculosis Fabry Disease Facial Hemiatrophy Facioscapulohumeral Muscular Dystrophy 1 Familial Mediterranean Fever Fanconi Anemia, Complementation Group E Fanconi Renotubular Syndrome 1 Fanconi Syndrome Fasciitis Fetal Akinesia Deformation Sequence Fibrosis of Extraocular Muscles, Congenital, 1 Fingerprint Body Myopathy Focal Myositis Foot Drop Frontotemporal Dementia Gastroesophageal Reflux Gastroparesis Germ Cells Tumors Gianotti Crosti Syndrome Giardioză Glaucoma-Related Pigment Dispersion Syndrome Glycerol Kinase Deficiency Glycogen Storage Disease Glycogen Storage Disease Ii Glycogen Storage Disease Iv Glycogen Storage Disease, Type Ixd Glycogen Storage Disease V Gne-Related Myopathy Gout Graft-Versus-Host Disease Graves' Disease Growth Hormone Deficiency Gyrate Atrophy of Choroid and Retina Headache Helix Syndrome Hemifacial Microsomia Hemolytic Anemia Hemophagocytic Lymphohistiocytosis, Familial, 1 Hepatic Adenomas, Familial Hepatitis Hepatitis a Hepatitis B Hepatitis C Hepatitis C Virus Hereditary Leiomyomatosis and Renal Cell Cancer Hereditary Myopathy with Early Respiratory Failure Hereditary Neuropathies Htlv-1 Associated Myelopathy/tropical Spastic Paraparesis Human Coronavirus Sensitivity Hydranencephaly Hydrocephalus Hydrops Fetalis, Nonimmune Hydrops, Lactic Acidosis, and Sideroblastic Anemia Hyperkalemic Periodic Paralysis Hypermethioninemia Hyperparathyroidism Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy Hyperthyroidism Hypertonia Hypertrophic Branchial Myopathy Hypertrophic Cardiomyopathy Hypertrophic Osteoarthropathy, Primary, Autosomal Recessive, 1 Hyperuricemia Hypokalemia Hypokalemic Periodic Paralysis, Type 1 Hypoparathyroidism Hypoparathyroidism, Sensorineural Deafness, and Renal Disease Hypophosphatasia Hypophosphatemia Hypospadias Hypotonia Ichthyosis Ichthyosis Prematurity Syndrome Ichthyosis Vulgaris Idiopathic Dropped Head Syndrome Idiopathic Inflammatory Myopathy Idiopathic Interstitial Pneumonia Immunoglobulin E Concentration, Serum Inclusion Body Myopathy with Paget Disease of Bone and Frontotemporal Dementia Inclusion Body Myositis Infantile Hypotonia Infertility Inflammatory Bowel Disease Inflammatory Leiomyosarcoma Inflammatory Myopathy with Abundant Macrophages Influenza Inherited Metabolic Disorder Insulin-Like Growth Factor I Intermediate Congenital Nemaline Myopathy Interstitial Lung Disease Interstitial Myocarditis Intestinal Pseudo-Obstruction Intrahepatic Cholestasis Intranuclear Rod Myopathy Intravascular Large B-Cell Lymphoma Ischemia Isolated Hyperckemia Juvenile Rheumatoid Arthritis Kearns-Sayre Syndrome Keloid Formation Keloids Lactic Acidosis Lama2-Related Muscular Dystrophy Lambert-Eaton Myasthenic Syndrome Lambert Syndrome Laryngeal Cleft Lateral Sclerosis Left Ventricular Noncompaction Left Ventricular Noncompaction 1 Leigh Syndrome Leiomyomatosis Leukemia Limb-Girdle Muscular Dystrophy Limb Ischemia Linear Scleroderma Lipid Storage Disease Lipodystrophy Lipodystrophy, Congenital Generalized, Type 4 Lipomatosis Lissencephaly 1 Localized Lipodystrophy Localized Scleroderma Locked-in Syndrome Long Qt Syndrome Lung Cancer Lung Disease Lupus Erythematosus Lymphoblastic Leukemia Lymphoma Lymphoplasmacytic Lymphoma Macrocephaly/megalencephaly Syndrome, Autosomal Recessive Macrophagic Myofasciitis Malignant Hyperthermia Malignant Hyperthermia 1 Malignant Hyperthermia Susceptibility Malignant Triton Tumor Mannose-Binding Lectin Deficiency Marden-Walker Syndrome Marfan Syndrome Marinesco-Sjogren Syndrome Mcleod Syndrome Megalencephaly Melanoma Melkersson-Rosenthal Syndrome Meningoencephalitis Mental Retardation-Hypotonic Facies Syndrome, X-Linked, 1 Mesenchymoma Metabolic Encephalomyopathic Crises, Recurrent, with Rhabdomyolysis, Cardiac Arrhythmias, and Neurodegeneration Microcephaly Microcolon Mitochondrial Complex Iii Deficiency Mitochondrial Disorders Mitochondrial Dna Depletion Syndrome 3 Mitochondrial Dna Depletion Syndrome 4a Mitochondrial Dna Depletion Syndrome 9 Mitochondrial Metabolism Disease Mitochondrial Myopathy Mitochondrial Myopathy, Encephalopathy, Lactic Acidosis, and Stroke-Like Episodes Mitochondrial Myopathy with Diabetes Mitochondrial Myopathy with Lactic Acidosis Mixed Connective Tissue Disease Mixed Germ Cell Tumor Miyoshi Muscular Dystrophy 1 Mohr-Tranebjaerg Syndrome Mononeuritis Multiplex Motor Neuron Disease Mucolipidosis Iv Mucositis Muir-Torre Syndrome Multicentric Reticulohistiocytosis Multiminicore Disease Multiple Acyl-Coa Dehydrogenase Deficiency Multiple Epiphyseal Dysplasia Multiple Mitochondrial Dysfunctions Syndrome 5 Multiple Pterygium Syndrome, Escobar Variant Multiple Sclerosis Multiple Symmetrical Lipomatosis Mungan Syndrome Muscle Disorders Muscle Tissue Disease Muscular Atrophy Muscular Dystrophy Muscular Dystrophy, Becker Type Muscular Dystrophy, Congenital, 1b Muscular Dystrophy, Congenital, Lmna-Related Muscular Dystrophy, Congenital, Megaconial Type Muscular Dystrophy, Congenital Merosin-Deficient, 1a Muscular Dystrophy, Duchenne Type Muscular Dystrophy-Dystroglycanopathy , Type a, 4 Muscular Dystrophy-Dystroglycanopathy , Type B, 5 Muscular Dystrophy-Dystroglycanopathy , Type C, 5 Muscular Dystrophy, Limb-Girdle, Type 1a Muscular Dystrophy, Limb-Girdle, Type 1b Muscular Dystrophy, Limb-Girdle, Type 1c Muscular Dystrophy, Limb-Girdle, Type 1e Muscular Dystrophy, Limb-Girdle, Type 1f 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 Muscular Dystrophy, Limb-Girdle, Type 2l Muscular Pseudohypertrophy-Hypothyroidism Syndrome Myasthenia Gravis Myeloid Leukemia Myocardial Infarction Myocarditis Myoclonus Myoclonus Epilepsy Myofibrillar Myopathy Myoglobinuria Myoglobinuria, Acute Recurrent, Autosomal Recessive Myoglobinuria, Recurrent Myopathy, Areflexia, Respiratory Distress, and Dysphagia, Early-Onset Myopathy, Centronuclear, 1 Myopathy, Centronuclear, 2 Myopathy, Centronuclear, X-Linked Myopathy, Congenital Myopathy, Congenital, with Fiber-Type Disproportion Myopathy, Distal, 1 Myopathy, Distal, 3 Myopathy, Distal, with Anterior Tibial Onset Myopathy, Lactic Acidosis, and Sideroblastic Anemia Myopathy, Lactic Acidosis, and Sideroblastic Anemia 1 Myopathy, Lactic Acidosis, and Sideroblastic Anemia 2 Myopathy, Mitochondrial Progressive, with Congenital Cataract, Hearing Loss, and Developmental Delay Myopathy, Myofibrillar, 1 Myopathy, Myofibrillar, 2 Myopathy, Myofibrillar, 3 Myopathy, Myofibrillar, 4 Myopathy, Myofibrillar, 6 Myopathy, Proximal, and Ophthalmoplegia Myopathy, Spheroid Body Myopathy - Thyrotoxic Myopathy, Tubular Aggregate, 1 Myopathy with Deficiency of Iron-Sulfur Cluster Assembly Enzyme Myopathy with Deficiency of Iscu Myopathy with Giant Abnormal Mitochondria Myopathy with Lactic Acidosis, Hereditary Myopathy, X-Linked, with Excessive Autophagy Myopathy, X-Linked, with Postural Muscle Atrophy Myopia Myosclerosis, Autosomal Recessive Myosinopathies Myosin Storage Myopathy Myositis Myotonia Myotonia Congenita Myotonic Disease Myotonic Dystrophy Myotonic Dystrophy 2 Myxedema Nail-Patella Syndrome Native American Myopathy Necrotizing Autoimmune Myopathy Nemaline Myopathy Nemaline Myopathy 1 Nemaline Myopathy 2 Nemaline Myopathy 3 Nemaline Myopathy 4 Nemaline Myopathy 5 Nephrogenic Systemic Fibrosis Nervous System Disease Neurodegeneration with Brain Iron Accumulation 2a Neurofibromatosis, Type Iv, of Riccardi Neuroleptic Malignant Syndrome Neuromuscular Disease Neuromyelitis Optica Neuromyelitis Optica Spectrum Disorder Neuronal Ceroid Lipofuscinosis Neuronitis Neuropathy Neurotrophic Keratopathy Neutral Lipid Storage Disease with Myopathy Neutropenia Nocardiosis Nonaka Myopathy Non-Involuting Congenital Hemangioma Obsessive-Compulsive Disorder Ocular Motility Disease Oculopharyngeal Muscular Dystrophy Oculopharyngodistal Myopathy Ogilvie Syndrome Osteochondritis Dissecans Osteomalacia Ovarian Cyst Pachygyria Pancreas Disease Pancytopenia Panniculitis Papular Mucinosis Paraneoplastic Syndromes Pearson Marrow-Pancreas Syndrome Peliosis Hepatis Pericarditis Peripheral Neuropathy, Myopathy, Hoarseness, and Hearing Loss Peroxisomal Disease Pfeiffer Syndrome Pharyngitis Phosphoglycerate Kinase Deficiency Phosphoglycerate Mutase Deficiency Phosphorylase Kinase Deficiency Pityriasis Rubra Pilaris Pneumonia Pneumothorax Poems Syndrome Poikiloderma, Hereditary Fibrosing, with Tendon Contractures, Myopathy, and Pulmonary Fibrosis Poland Syndrome Poliomyelitis Polyarteritis Nodosa Polydactyly, Postaxial, with Progressive Myopia Polyglucosan Body Myopathy 1 with or Without Immunodeficiency Polyglucosan Body Myopathy 2 Polymyositis Polyneuropathy Polyradiculopathy Portal Vein Thrombosis Postpoliomyelitis Syndrome Primary Biliary Cirrhosis Primary Hyperparathyroidism Prion Disease Progressive External Ophthalmoplegia with Mitochondrial Dna Deletions, Autosomal Dominant 2 Progressive External Ophthalmoplegia with Mitochondrial Dna Deletions, Autosomal Dominant 3 Progressive External Ophthalmoplegia with Mitochondrial Dna Deletions, Autosomal Dominant 4 Progressive External Ophthalmoplegia with Mitochondrial Dna Deletions, Autosomal Recessive 1 Progressive Myoclonus Epilepsy Proteus Syndrome Proximal Myopathy with Focal Depletion of Mitochondria Pseudoachondroplasia Psoriasis Psoriasis 13 Ptosis Pulmonary Fibrosis Pure Mitochondrial Myopathy Pyoderma Pyoderma Gangrenosum Pyomyositis Pyruvate Kinase Deficiency of Red Cells Quadriplegia Reducing Body Myopathy Renal Glucosuria Renal Hypodysplasia/aplasia 1 Renal Tubular Acidosis Respiratory Failure Restrictive Cardiomyopathy Retinal Degeneration Retinitis Reye Syndrome Rhabdomyosarcoma Rheumatoid Arthritis Rheumatoid Vasculitis Riboflavin Transporter Deficiency Rigid Spine Muscular Dystrophy 1 Rippling Muscle Disease 2 Ruvalcaba Syndrome Sakati Syndrome Salih Myopathy Sarcoidosis 2 Scapuloperoneal Myopathy Scapuloperoneal Myopathy, Myh7-Related Scapuloperoneal Myopathy, X-Linked Dominant Scheie Syndrome Schizoaffective Disorder Schizophrenia Scleromyxedema Scoliosis Scott Syndrome Secretory Diarrhea Seminoma Sensorineural Hearing Loss Sensory Ataxic Neuropathy, Dysarthria, and Ophthalmoparesis Severe Congenital Nemaline Myopathy Sheehan Syndrome Shwachman-Diamond Syndrome Sideroblastic Anemia Sjogren Syndrome Skeletal Dysplasias Sleep Apnea Spastic Diplegia Spasticity Spastic Paraparesis Spinal Muscular Atrophy Spinal Muscular Atrophy, Type Ii Spindle Cell Rhabdomyosarcoma Spondylitis Spondyloarthropathy 1 Spondylocarpotarsal Synostosis Syndrome Spondyloocular Syndrome Status Asthmaticus Status Epilepticus Steatitis Steatorrhea Stormorken Syndrome Subacute Thyroiditis Superior Mesenteric Artery Syndrome Swallowing Disorders Systemic Lupus Erythematosus Systolic Heart Failure Temporomandibular Ankylosis Tendinopathy Tetralogy of Fallot Thalassemia Thrombocytopenia Thrombosis Thymic Hyperplasia Thymoma Thyroiditis Thyrotoxic Exophthalmos Thyrotoxic Periodic Paralysis Tibial Muscular Dystrophy Tooth Disease Toxoplasmoză Trabecular Myopathy Trichinosis Triosephosphate Isomerase Deficiency Tropical Spastic Paraparesis Typical Congenital Nemaline Myopathy Tyrosinemia Tyrosinemia, Type I Ullrich Congenital Muscular Dystrophy 1 Uremia Vasculitis Vici Syndrome Visceral Myopathy Visceral Myopathy, Familial, with External Ophthalmoplegia Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 6 Walker-Warburg Syndrome Welander Distal Myopathy Welander Distal Myopathy, Swedish Type Wild Type Attr Amyloidosis Williams-Beuren Syndrome Wilson-Turner X-Linked Mental Retardation Syndrome Xanthomatosis Zebra Body Myopathy Zellweger Syndrome