Informaţii despre

Nume Neuromuscular Disease
Pagina Web www.malacards.org
Clasificari ICD10 Myoneural disorder, unspecified; Neuromuscular dysfunction of bladder, unspecified
Clasificare anatomică Malacards Boli nefrologice (ale rinichilor); Boli neuronale

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Boli A-Z Aging Alexithymia Alopecia, Neurologic Defects, and Endocrinopathy Syndrome Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity Al-Raqad Syndrome Aniridia 1 Anorexia Nervosa 1 Arrhythmogenic Right Ventricular Cardiomyopathy Arthrochalasia Ehlers-Danlos Syndrome Arthrogryposis Multiplex Congenita, Neurogenic, with Myelin Defect Ataxia and Polyneuropathy, Adult-Onset Atrial Standstill 1 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 Breast Cancer Brody Myopathy Burns Cardiomyopathy, Dilated, 1a Cardiomyopathy, Dilated, 1b Cardioneuromyopathy with Hyaline Masses and Nemaline Rods Cataract Central Core Disease of Muscle Centronuclear Myopathy Cervicitis Charcot-Marie-Tooth Disease Charcot-Marie-Tooth Disease, Axonal, Type 2l Charcot-Marie-Tooth Disease, Demyelinating, Type 1b Charcot-Marie-Tooth Disease, Demyelinating, Type 1f Charcot-Marie-Tooth Disease, Dominant Intermediate B Charcot-Marie-Tooth Neuropathy Type 1 Cholestasis Chronic Inflammatory Demyelinating Polyradiculoneuropathy Chronic Pain Cleft Palate, Isolated Clubfoot Congenital Fiber-Type Disproportion Craniosynostosis 1 Cyclic Vomiting Syndrome Cystic Fibrosis Cytoplasmic Body Myopathy Dementia Distal Muscular Dystrophy Dysphagia Emery-Dreifuss Muscular Dystrophy 1, X-Linked Encephalitis Encephalopathy Endometriosis Epidermolysis Bullosa Epidermolysis Bullosa Simplex Epidermolysis Bullosa Simplex, Generalized Epilepsy Extracardiac Rhabdomyoma Familial Periodic Paralysis Fanconi Anemia, Complementation Group E Foot Drop Frontotemporal Dementia Glycogen Storage Disease Ii Glycogen Storage Disease Iii Glycogen Storage Disease V Hepatic Adenomas, Familial Hereditary Neuropathy with Liability to Pressure Palsy Hypertonia Hypoxia Inclusion Body Myositis Influenza Intrahepatic Cholestasis Juvenile Spinal Muscular Atrophy Lagophthalmos Lambert-Eaton Myasthenic Syndrome Large Cell Neuroendocrine Carcinoma Laryngitis Lateral Sclerosis Limb-Girdle Muscular Dystrophy Lmna-Related Cardiocutaneous Progeria Syndrome Malignant Hyperthermia Microcolon Motor Neuron Disease Multiple Sclerosis Muscle Tissue Disease Muscular Atrophy Muscular Dystrophy Muscular Dystrophy, Becker Type Muscular Dystrophy, Congenital, 1b Muscular Dystrophy, Congenital Merosin-Deficient, 1a Muscular Dystrophy, Duchenne Type Muscular Dystrophy-Dystroglycanopathy , Type B, 6 Muscular Dystrophy-Dystroglycanopathy , Type C, 5 Myasthenia Gravis Myofibrillar Myopathy Myopathy Myopathy, Centronuclear, X-Linked Myopathy, Congenital Myopathy, Proximal, and Ophthalmoplegia Myopathy, X-Linked, with Excessive Autophagy Myositis Myotonia Myotonia Congenita Myotonic Disease Myotonic Dystrophy Nemaline Myopathy Nervous System Disease Neuronitis Neuropathy Neuropathy, Congenital Hypomyelinating or Amyelinating, Autosomal Recessive Neuropathy, Hereditary, with Liability to Pressure Palsies Oculopharyngodistal Myopathy Parathyroid Gland Disease Pentosuria Peripheral Nervous System Disease Pleural Disease Pneumothorax Poliomyelitis Polyradiculoneuropathy Progressive Muscular Atrophy Proximal Spinal Muscular Atrophy Ptosis Pulmonary Emphysema Pulmonary Fibrosis Reducing Body Myopathy Renal Hypodysplasia/aplasia 1 Respiratory Failure Rigid Spine Muscular Dystrophy 1 Roussy-Levy Hereditary Areflexic Dystasia Scoliosis Sleep Disorder Spasticity Spinal Cord Injury Spinal Disease Spinal Muscular Atrophy Spinal Muscular Atrophy, Type I Spinal Muscular Atrophy, Type Ii Spinal Muscular Atrophy, Type Iii Spinal Muscular Atrophy, Type Iv Spinal Stenosis Survival Motor Neuron Spinal Muscular Atrophy Swallowing Disorders