Informaţii despre

Nume Muscular Dystrophy, Congenital, Lmna-Related
Pagina Web www.malacards.org
Clasificare globală Malacards Boli genetice; Boli rare
Clasificari ICD10 Congenital myopathies
Clasificare anatomică Malacards Boli musculare; Boli neuronale

Vezi şi

Boli A-Z Ablepharon-Macrostomia Syndrome Aging Alopecia, Neurologic Defects, and Endocrinopathy Syndrome Alport Syndrome, X-Linked Al-Raqad Syndrome Aneurysm of Sinus of Valsalva Aniridia 1 Anorexia Nervosa 1 Arterial Tortuosity Syndrome 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 Atrioventricular Block Autosomal Dominant Limb-Girdle Muscular Dystrophy Autosomal Recessive Limb-Girdle Muscular Dystrophy Bethlem Myopathy 1 Blood Group--Ahonen Blood Group, I System Cardiac Arrhythmia Cardiomyopathy, Dilated, 1a Cardiomyopathy, Dilated, 1b Cardiomyopathy, Dilated, 1e Cardiomyopathy, Dilated, 1h Cataract Cerebellar Hypoplasia Cerebritis Choroiditis Collagen Vi-Related Myopathy Congenital Fiber-Type Disproportion Congenital Muscular Dystrophy Type 1a Congenital Muscular Dystrophy with Cerebellar Involvement Congenital Muscular Dystrophy with Intellectual Disability Congenital Muscular Dystrophy Without Intellectual Disability Craniometaphyseal Dysplasia, Autosomal Dominant Diabetes Mellitus Dystrophinopathies Ehlers-Danlos Syndrome Emerinopathy Emery-Dreifuss Muscular Dystrophy Emery-Dreifuss Muscular Dystrophy 2, Autosomal Dominant Epidermolysis Bullosa Epidermolysis Bullosa, Junctional, Herlitz Type Epidermolysis Bullosa Simplex Epilepsy Epithelial Recurrent Erosion Dystrophy Familial Partial Lipodystrophy Fukuyama Type Muscular Dystrophy Hydrocephalus Hyperekplexia Hypoglycemia Hypotonia Infantile Scoliosis Joubert Syndrome 1 Junctional Epidermolysis Bullosa Laryngeal Cleft Laryngitis Leigh Syndrome Leukodystrophy Limb-Girdle Muscular Dystrophy Lissencephaly Long Qt Syndrome Macroglossia Microcephaly Miller-Dieker Lissencephaly Syndrome Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly Muscle Disorders Muscle Eye Brain Disease Muscle Tissue Disease Muscular Atrophy Muscular Dystrophy Muscular Dystrophy, Becker Type Muscular Dystrophy, Congenital, 1b Muscular Dystrophy, Congenital, Megaconial Type Muscular Dystrophy, Congenital Merosin-Deficient, 1a Muscular Dystrophy, Congenital, Producing Arthrogryposis 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, 2 Muscular Dystrophy-Dystroglycanopathy , Type C, 4 Muscular Dystrophy-Dystroglycanopathy , Type C, 5 Muscular Dystrophy, Limb-Girdle, Type 1b Muscular Dystrophy, Limb-Girdle, Type 2l Myocarditis Myopathy Myopathy, Congenital Myopathy, Proximal, and Ophthalmoplegia Myotonic Dystrophy Nervous System Disease Neuronal Migration Disorders Neuronitis Neuropathy Neuropathy, Hereditary Sensory and Autonomic, Type Iii Parkinson Disease 15, Autosomal Recessive Early-Onset Pelger-Huet Anomaly Polyglucosan Body Myopathy 1 with or Without Immunodeficiency Polymicrogyria Pontocerebellar Hypoplasia Proximal Myopathy with Focal Depletion of Mitochondria Ptosis Retinitis Rigid Spine Muscular Dystrophy 1 Salih Myopathy Scoliosis Seizure Disorder Skeletal Muscle Cancer Spinal Muscular Atrophy Supravalvular Aortic Stenosis Syringomyelia Tetraamelia Syndrome, Autosomal Recessive Ullrich Congenital Muscular Dystrophy 1 Undifferentiated Pleomorphic Sarcoma Walker-Warburg Syndrome West Syndrome