Informaţii despre

Nume Muscular Dystrophy
Pagina Web www.malacards.org
Clasificare globală Malacards Boli genetice; Boli rare
Clasificari ICD10 Muscular dystrophy
Clasificare anatomică Malacards Boli cardiovasculare; Boli musculare; Boli neuronale
Boli din aceeaşi familie Congenital Muscular Dystrophy Due to Dystroglycanopathy; Congenital Muscular Dystrophy Type 1a; Muscular Dystrophy, Congenital, 1b

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Boli A-Z 18p Deletion Syndrome Ablepharon-Macrostomia Syndrome Achondroplasia Acid-Labile Subunit Deficiency Acute Monoblastic Leukemia Adenosine Deaminase Deficiency Adie Pupil Aging Aland Island Eye Disease Albinism 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 Alzheimer Disease 3 Aminoaciduria Amyloidosis Amyotonia Congenita Anauxetic Dysplasia 1 Androgen Insensitivity Syndrome, Mild Aneurysm Aneurysm of Sinus of Valsalva Angelman Syndrome Angioedema Aniridia 1 Anorexia Nervosa 1 Apocrine Gland Secretion, Variation in Arachnoid Cysts Arachnoiditis Arrhythmogenic Right Ventricular Cardiomyopathy Arthritis Arthrochalasia Ehlers-Danlos Syndrome Arthrogryposis Multiplex Congenita, Neurogenic, with Myelin Defect Ataxia and Polyneuropathy, Adult-Onset Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus Atherosclerosis Susceptibility Atrial Fibrillation Atrial Standstill Atrioventricular Block Attention Deficit-Hyperactivity Disorder Atypical Lipomatous Tumor Aural Atresia, Congenital Autism Autism Spectrum Disorder Autonomic Dysfunction Autosomal Dominant Limb-Girdle Muscular Dystrophy Autosomal Dominant Limb-Girdle Muscular Dystrophy Type 1c Autosomal Dominant Limb-Girdle Muscular Dystrophy Type 1g 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 Back Pain Basilar Artery Occlusion Behr Syndrome Bethlem Myopathy 1 Birdshot Chorioretinopathy Bleeding Disorder, Platelet-Type, 11 Blind Loop Syndrome 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 Cancer Bone Fracture Bone Mineral Density Quantitative Trait Locus 15 Bone Mineral Density Quantitative Trait Locus 8 Bosma Arhinia Microphthalmia Syndrome Breast Cancer Brittle Bone Disorder Camptocormism Cardiac Arrest Cardiac Arrhythmia Cardiac Conduction Defect Cardiac Tamponade Cardiomyopathy, Dilated, 1a Cardiomyopathy, Dilated, 1b Cardiomyopathy, Dilated, 3b Cardioneuromyopathy with Hyaline Masses and Nemaline Rods Cataract Cataract 4, Multiple Types Caveolinopathies Central Core Disease of Muscle Centronuclear Myopathy Cerebellar Hypoplasia Cerebral Palsy Cerebritis Charcot-Marie-Tooth Disease Chilaiditi Syndrome Chorea, Childhood-Onset, with Psychomotor Retardation Choreatic Disease Choroiditis Chromosome 9p Deletion Syndrome Chromosome Xp21 Deletion Syndrome Chronic Granulomatous Disease Chronic Pain Clostridium Difficile Colitis Coats Disease Colitis Collagen Disease Collagen Vi Related Muscular Dystrophy Collagen Vi-Related Myopathy Color Blindness Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy Congenital Fiber-Type Disproportion Congenital Generalized Lipodystrophy Congenital Hepatic Fibrosis Congenital Muscular Dystrophy Type 1a Congenital Muscular Dystrophy with Cerebellar Involvement Congenital Muscular Dystrophy with Intellectual Disability Congenital Muscular Dystrophy Without Intellectual Disability Congenital Myasthenic Syndrome Congenital Stationary Night Blindness Congestive Heart Failure Creatine Phosphokinase, Elevated Serum Cystic Fibrosis Cytidine Monophospho-N-Acetylneuraminic Acid Hydroxylase, Pseudogene Cytoplasmic Body Myopathy Deafness, Autosomal Dominant Nonsyndromic Sensorineural 3 Dementia Dermatomyositis Desmoid Tumor Dfnb1 Diabetes Mellitus Diamond-Blackfan Anemia Dilated Cardiomyopathy Distal Muscular Dystrophy Duane Retraction Syndrome Dwarfism Dysferlinopathy Dyskeratosis Congenita Dysphagia Dystonia Dystrophinopathies Early-Onset Generalized Limb-Onset Dystonia Egg Allergy Ehlers-Danlos Syndrome Embryonal Rhabdomyosarcoma Emerinopathy Emery-Dreifuss Muscular Dystrophy Emery-Dreifuss Muscular Dystrophy 2, Autosomal Dominant Emery-Dreifuss Muscular Dystrophy 3, Autosomal Recessive Emery-Dreifuss Muscular Dystrophy, X-Linked Emery-Dreifuss Syndrome Encephalomalacia Encephalomyopathy Encephalopathy Endotheliitis Epidermolysis Bullosa Epidermolysis Bullosa, Junctional, Herlitz Type Epidermolysis Bullosa Simplex Epidermolysis Bullosa Simplex with Muscular Dystrophy Epilepsy Epileptic Encephalopathy, Early Infantile, 36 Epithelial Recurrent Erosion Dystrophy Esterase C Extracardiac Rhabdomyoma Facioscapulohumeral Muscular Dystrophy 1 Facioscapulohumeral Muscular Dystrophy 2 Familial Adenomatous Polyposis Familial Partial Lipodystrophy Fanconi Anemia, Complementation Group E Fatty Liver Disease Focal Myositis Foot Drop Fragile X Syndrome Frontotemporal Dementia Fukuyama Type Muscular Dystrophy Gastric Dilatation Gianotti Crosti Syndrome Glycerol Kinase Deficiency Growth Hormone Deficiency Helix Syndrome Hemophagocytic Lymphohistiocytosis, Familial, 1 Hemophilia Hemophilia a Hepatic Adenomas, Familial Hepatitis Hereditary Neuropathies Hereditary Neuropathy with Liability to Pressure Palsy Hip Subluxation Hydrocephalus Hydrops, Lactic Acidosis, and Sideroblastic Anemia Hyperekplexia Hypersomnia Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy Hypertrophic Cardiomyopathy Hypoadrenocorticism, Familial Hypoglycemia Hypogonadism Hypotonia Hypotonic Sclerotic Muscular Dystrophy Ichthyosis Ichthyosis Prematurity Syndrome Ichthyosis Vulgaris Idiopathic Inflammatory Myopathy Immune Suppression Immunoglobulin E Concentration, Serum Inclusion Body Myositis Infantile Scoliosis Influenza Insulin-Like Growth Factor I Intellectual Disability-Developmental Delay-Contractures Syndrome Intervertebral Disc Disease Intracranial Hypertension Ischemia Isolated Hyperckemia Joubert Syndrome 1 Junctional Epidermolysis Bullosa Juvenile Polymyositis Lama2-Related Muscular Dystrophy Laryngeal Cleft Laryngitis Lateral Sclerosis Leber Congenital Amaurosis 4 Left Ventricular Noncompaction Leigh Syndrome Leukemia Leukodystrophy Limb-Girdle Muscular Dystrophy Limb-Girdle Muscular Dystrophy, Type 1g Lipodystrophy Liposarcoma Lissencephaly Liver Disease Localized Lipodystrophy Long Qt Syndrome Lymphoma Macroglossia Macrophagic Myofasciitis Macular Dystrophy, Vitelliform, 2 Major Affective Disorder 2 Mal De Meleda Malignant Hyperthermia Malignant Hyperthermia Susceptibility Mcleod Syndrome Medulloblastoma Meester-Loeys Syndrome Megacolon Meningitis Microcephaly Microphthalmia Miller-Dieker Lissencephaly Syndrome Mitochondrial Disorders Mitochondrial Encephalomyopathy Mitochondrial Myopathy Miyoshi Muscular Dystrophy 1 Miyoshi Muscular Dystrophy 3 Mucolipidosis Ii Alpha/beta Multiminicore Disease Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly Multiple Mitochondrial Dysfunctions Syndrome 5 Multiple Sclerosis Muscle Disorders Muscle Eye Brain Disease Muscle Hypertrophy Muscle Tissue Disease Muscular Atrophy 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, Congenital, Producing Arthrogryposis Muscular Dystrophy, Duchenne and Becker Type Muscular Dystrophy, Duchenne Type Muscular Dystrophy-Dystroglycanopathy Muscular Dystrophy-Dystroglycanopathy , Type a, 1 Muscular Dystrophy-Dystroglycanopathy , Type a, 4 Muscular Dystrophy-Dystroglycanopathy , Type B, 5 Muscular Dystrophy-Dystroglycanopathy , Type B, 6 Muscular Dystrophy-Dystroglycanopathy , Type C, 1 Muscular Dystrophy-Dystroglycanopathy , Type C, 14 Muscular Dystrophy-Dystroglycanopathy , Type C, 2 Muscular Dystrophy-Dystroglycanopathy , Type C, 3 Muscular Dystrophy-Dystroglycanopathy , Type C, 4 Muscular Dystrophy-Dystroglycanopathy , Type C, 5 Muscular Dystrophy-Dystroglycanopathy , Type C, 7 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 1h 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 Dystrophy, Limb-Girdle, Type 2q Muscular Dystrophy, Limb-Girdle, Type 2r Muscular Dystrophy, Limb-Girdle, Type 2w Myasthenia Gravis Myelodysplastic Syndrome Myeloid Leukemia Myelomeningocele Myocarditis Myoclonus Myofibrillar Myopathy Myoglobinuria Myoglobinuria, Acute Recurrent, Autosomal Recessive Myopathy Myopathy, Congenital Myopathy, Distal, with Anterior Tibial Onset Myopathy, Myofibrillar, 1 Myopathy, Myofibrillar, 3 Myopathy, Proximal, and Ophthalmoplegia Myopathy, Spheroid Body Myositis Myotonia Myotonic Dystrophy Myxedema Necrotizing Autoimmune Myopathy Nephrolithiasis Nephrolithiasis, X-Linked Recessive, with Renal Failure Nervous System Disease Neuromuscular Disease Neuromyelitis Optica Neuronal Migration Disorders Neuronitis Neuropathy Neuropathy, Hereditary Sensory and Autonomic, Type Iii Neuropathy, Hereditary, with Liability to Pressure Palsies Neutrophil Actin Dysfunction Night Blindness Nondystrophic Myotonia Nonsyndromic Deafness Ocular Albinism Ocular Muscular Dystrophy Oculopharyngeal Muscular Dystrophy Oculopharyngodistal Myopathy Olivopontocerebellar Atrophy Papilledema Parkinson Disease 15, Autosomal Recessive Early-Onset Patent Foramen Ovale Pectus Excavatum Pelger-Huet Anomaly Pentosuria Pericardial Effusion Peripartum Cardiomyopathy Pharyngitis Phelan-Mcdermid Syndrome Plexopathy Polyglucosan Body Myopathy 1 with or Without Immunodeficiency Polyhydramnios Polymicrogyria Polymyositis Polyneuropathy Pontocerebellar Hypoplasia Postpoliomyelitis Syndrome Prader-Willi Syndrome Progressive Familial Heart Block, Type Ib Progressive Muscular Atrophy Protein C Deficiency Proximal Myopathy with Focal Depletion of Mitochondria Proximal Spinal Muscular Atrophy Ptosis Pulmonary Valve Stenosis Pyloric Atresia Quadriplegia Reducing Body Myopathy Renal Hypodysplasia/aplasia 1 Restless Legs Syndrome Retinal Vascular Disease Retinitis Retinitis Pigmentosa Rhabdomyosarcoma Rhabdomyosarcoma, Embryonal, 1 Right Bundle Branch Block Rigid Spine Muscular Dystrophy 1 Salih Myopathy Sarcosinemia Scapuloperoneal Myopathy, Myh7-Related Schizophrenia Scoliosis Scoliosis, Isolated 2 Seizure Disorder Skeletal Dysplasias Sleep Apnea Sleep Disorder Spasticity Spastic Paraparesis Spinal and Bulbar Muscular Atrophy, X-Linked 1 Spinal Cord Injury Spinal Muscular Atrophy Spinal Muscular Atrophy, Type Ii Spiradenoma Spondyloocular Syndrome Squamous Cell Carcinoma Supravalvular Aortic Stenosis Syringomyelia Telangiectasis Three M Syndrome 1 Thrombosis Tibial Muscular Dystrophy Toe Syndactyly, Telecanthus, and Anogenital and Renal Malformations Tooth Disease Toxic Megacolon Tracheobronchomalacia Transmitted_by Treacher Collins Syndrome 1 Tricuspid Atresia Tuberculous Meningitis Ullrich Congenital Muscular Dystrophy 1 Vacuolar Neuromyopathy Vaginitis Vascular Disease Walker-Warburg Syndrome Well-Differentiated Liposarcoma West Syndrome Wolff-Parkinson-White Syndrome