Informaţii despre

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

Vezi şi

Boli A-Z Adie Pupil Alopecia, Neurologic Defects, and Endocrinopathy Syndrome Alport Syndrome, X-Linked Al-Raqad Syndrome Androgen Insensitivity Syndrome, Mild Aniridia 1 Anorexia Nervosa 1 Arthrochalasia Ehlers-Danlos Syndrome Arthrogryposis Multiplex Congenita, Neurogenic, with Myelin Defect Aspiration Pneumonia Benign Autosomal Dominant Myopathy Bethlem Myopathy 1 Blood Group--Ahonen Blood Group, Dombrock System Blood Group, I System Brachial Plexus Neuritis Brody Myopathy Cap Myopathy Cardiac Conduction Defect Cardioneuromyopathy with Hyaline Masses and Nemaline Rods Carey-Fineman-Ziter Syndrome Central Core Disease of Muscle Central Core Myopathy Centronuclear Myopathy Charcot-Marie-Tooth Disease, Dominant Intermediate B Childhood-Onset Nemaline Myopathy Communicating Hydrocephalus Congenital Fiber-Type Disproportion Congenital Myasthenic Syndrome Congenital Structural Myopathy Craniosynostosis Cutis Laxa Diarrhea Distal Muscular Dystrophy Encephalopathy Fetal Akinesia Deformation Sequence Foot Drop Gne-Related Myopathy Hepatic Adenomas, Familial Hydrocephalus Hypotonia Inclusion Body Myositis Intermediate Congenital Nemaline Myopathy Limb-Girdle Muscular Dystrophy Malignant Hyperthermia Malignant Hyperthermia Susceptibility Marden-Walker Syndrome Microcephaly Multiminicore Disease Multiple Pterygium Syndrome, Lethal Type Muscle Disorders Muscle Tissue Disease Muscular Atrophy Muscular Dystrophy Muscular Dystrophy, Becker Type Muscular Dystrophy, Congenital, Lmna-Related Muscular Dystrophy, Duchenne Type Muscular Dystrophy-Dystroglycanopathy , Type a, 4 Myopathy Myopathy, Centronuclear, 1 Myopathy, Centronuclear, X-Linked Myopathy, Congenital, with Fiber-Type Disproportion Myopathy Due to Malate-Aspartate Shuttle Defect Myopathy, Myofibrillar, 2 Myopia Myositis Myotonia Myotonia Congenita Myotonic Dystrophy Native American Myopathy Nemaline Myopathy Nemaline Myopathy 4 Neurodegeneration with Brain Iron Accumulation 2a Neuromuscular Disease Neuropathy Pachygyria Pneumonia Polyglucosan Body Myopathy 1 with or Without Immunodeficiency Reducing Body Myopathy Rigid Spine Muscular Dystrophy 1 Scapuloperoneal Myopathy Scoliosis Secretory Diarrhea Severe Congenital Nemaline Myopathy Spinal Muscular Atrophy Spinal Muscular Atrophy, Type Ii Spondyloocular Syndrome Typical Congenital Nemaline Myopathy Zebra Body Myopathy