Informaţii despre

Nume Muscular Dystrophy, Duchenne Type
Pagina Web www.malacards.org
Clasificare globală Malacards Boli genetice; Boli rare
Clasificari ICD10 Muscular dystrophy
Clasificare anatomică Malacards Boli ale ochiului; Boli musculare; Boli neuronale

Vezi şi

Boli A-Z Achondroplasia Acute Monoblastic Leukemia Acute Myocardial Infarction Adenosine Deaminase Deficiency Adie Pupil Adrenal Hypoplasia, Congenital Aging Alacrima, Achalasia, and Mental Retardation Syndrome Aland Island Eye Disease Albinism Alopecia, Neurologic Defects, and Endocrinopathy Syndrome Alport Syndrome, X-Linked Al-Raqad Syndrome Aneurysm Aniridia 1 Anorexia Nervosa 1 Arterial Tortuosity Syndrome Arthrochalasia Ehlers-Danlos Syndrome Arthrogryposis Multiplex Congenita, Neurogenic, with Myelin Defect Attention Deficit-Hyperactivity Disorder Autism Autism Spectrum Disorder Autonomic Dysfunction 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 Back Pain Basilar Artery Occlusion Bleeding Disorder, Platelet-Type, 11 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 Bone Fracture Bone Mineral Density Quantitative Trait Locus 15 Bone Mineral Density Quantitative Trait Locus 8 Breast Rhabdomyosarcoma Brittle Bone Disorder Cardiac Tamponade Cardiomyopathy, Dilated, 1a Cardiomyopathy, Dilated, 1b Cardiomyopathy, Dilated, 1d Cardiomyopathy, Dilated, 3b Cardioneuromyopathy with Hyaline Masses and Nemaline Rods Cerebral Palsy Cerebritis Charcot-Marie-Tooth Disease Chilaiditi Syndrome Chromosome Xp21 Deletion Syndrome Chronic Granulomatous Disease Chronic Pain Clostridium Difficile Colitis Coats Disease Colitis Collagen Disease Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy Congenital Stationary Night Blindness Congestive Heart Failure Creatine Phosphokinase, Elevated Serum Cystic Fibrosis Cytidine Monophospho-N-Acetylneuraminic Acid Hydroxylase, Pseudogene Cytoplasmic Body Myopathy Dermatomyositis Diamond-Blackfan Anemia Dilated Cardiomyopathy Distal Muscular Dystrophy Duane Retraction Syndrome Dysphagia Dystrophinopathies Egg Allergy Endotheliitis Epilepsy Familial Isolated Dilated Cardiomyopathy Familial Isolated Restrictive Cardiomyopathy Fanconi Anemia, Complementation Group E Fatty Liver Disease Fragile X Syndrome Gas Gangrene Gastric Dilatation Glycerol Kinase Deficiency Hemophagocytic Lymphohistiocytosis, Familial, 1 Hemophilia Hemophilia a Hepatic Adenomas, Familial Hip Subluxation Hydrocephalus Hydrops, Lactic Acidosis, and Sideroblastic Anemia Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy Hypertrophic Cardiomyopathy Hypoadrenocorticism, Familial Ichthyosis Ichthyosis Prematurity Syndrome Ichthyosis Vulgaris Immune Suppression Inclusion Body Myositis Influenza Interstitial Myocarditis Intervertebral Disc Disease Intracranial Hypertension Intrinsic Cardiomyopathy Ischemia Isolated Hyperckemia Laryngeal Cleft Lateral Sclerosis Left Ventricular Noncompaction Leukemia Limb-Girdle Muscular Dystrophy Liver Disease Macroglossia Macular Dystrophy, Vitelliform, 2 Major Affective Disorder 2 Malignant Hyperthermia Malignant Triton Tumor Mcleod Syndrome Medulloblastoma Megacolon Mesenchymoma Metabolic Encephalomyopathic Crises, Recurrent, with Rhabdomyolysis, Cardiac Arrhythmias, and Neurodegeneration Muscle Eye Brain Disease Muscle Hypertrophy Muscle Tissue Disease Muscular Atrophy Muscular Dystrophy Muscular Dystrophy, Becker Type Muscular Dystrophy, Congenital, 1b Muscular Dystrophy, Congenital, Lmna-Related Muscular Dystrophy, Congenital Merosin-Deficient, 1a Muscular Dystrophy, Duchenne and Becker Type Muscular Dystrophy-Dystroglycanopathy , Type a, 4 Muscular Dystrophy-Dystroglycanopathy , Type B, 5 Muscular Dystrophy-Dystroglycanopathy , Type B, 6 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 Myelomeningocele Myocarditis Myoglobinuria Myoglobinuria, Acute Recurrent, Autosomal Recessive Myopathy Myopathy, Proximal, and Ophthalmoplegia Myositis Myotonia Myotonic Dystrophy Neonatal Myasthenia Gravis Nephrolithiasis Nephrolithiasis, X-Linked Recessive, with Renal Failure Nervous System Disease Neuroleptic Malignant Syndrome Neuromuscular Disease Neuronitis Neuropathy Night Blindness Ocular Albinism Olivopontocerebellar Atrophy Patent Foramen Ovale Pericardial Effusion Peripartum Cardiomyopathy Phelan-Mcdermid Syndrome Pleomorphic Rhabdomyosarcoma Polyglucosan Body Myopathy 1 with or Without Immunodeficiency Polyhydramnios Polymyositis Postpoliomyelitis Syndrome Prader-Willi Syndrome Prostate Rhabdomyosarcoma Reducing Body Myopathy Restless Legs Syndrome Restrictive Cardiomyopathy Retinitis Retinitis Pigmentosa Rhabdomyosarcoma Rigid Spine Muscular Dystrophy 1 Sarcosinemia Scoliosis Skeletal Dysplasias Sleep Disorder Spinal Cord Injury Spinal Muscular Atrophy Spinal Muscular Atrophy, Type Ii Spindle Cell Rhabdomyosarcoma Spiradenoma Thrombosis Tick Paralysis Toe Syndactyly, Telecanthus, and Anogenital and Renal Malformations Tooth Disease Toxic Megacolon Tracheobronchomalacia Transmitted_by Undifferentiated Pleomorphic Sarcoma Virus Associated Hemophagocytic Syndrome Walker-Warburg Syndrome Wolff-Parkinson-White Syndrome X-Linked Disease