Informaţii despre

Nume Polyglucosan Body Myopathy 1 with or Without Immunodeficiency
Pagina Web www.malacards.org
Clasificare globală Malacards Boli genetice; Boli metabolice; Boli rare
Clasificari ICD10 Glycogen storage disease
Clasificare anatomică Malacards Boli ale sistemului imunitar; Boli de sânge; Boli neuronale; Boli osoase

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Boli A-Z 3-Methylglutaconic Aciduria Acute Motor and Sensory Axonal Neuropathy Acute Respiratory Distress Syndrome Adult Dermatomyositis Aging Al Amyloidosis 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 Amyloidosis Andersen Cardiodysrhythmic Periodic Paralysis Aniridia 1 Anorexia Nervosa 1 Argyria Arthritis Arthrochalasia Ehlers-Danlos Syndrome Arthrogryposis Multiplex Congenita, Neurogenic, with Myelin Defect Ataxia and Polyneuropathy, Adult-Onset Autosomal Recessive Limb-Girdle Muscular Dystrophy Axonal Neuropathy Bethlem Myopathy 1 Blood Group--Ahonen Blood Group, I System Breast Cancer Brittle Bone Disorder Cap Myopathy Cardiac Arrhythmia Cataract Centronuclear Myopathy Cerebral Palsy Cerebritis Cervicitis Charcot-Marie-Tooth Disease Chronic Polyneuropathy Chronic Progressive External Ophthalmoplegia Congenital Contractures Congenital Myasthenic Syndrome Conn's Syndrome Critical Illness Polyneuropathy Danon Disease Dermatomyositis Diabetic Neuropathy Diabetic Polyneuropathy Dilated Cardiomyopathy Distal Arthrogryposis Distal Muscular Dystrophy Dysphagia Ehlers-Danlos Syndrome Ehlers-Danlos Syndrome, Classic-Like Encephalitis End Stage Renal Failure Epilepsy Estrogen-Receptor Negative Breast Cancer Familial Periodic Paralyses Familial Periodic Paralysis Fanconi Syndrome Glycogen Storage Disease Glycogen Storage Disease Iv Graft-Versus-Host Disease Hypokalemia Hypokalemic Periodic Paralysis, Type 1 Hypophosphatemia Hypotonia Idiopathic Spinal Cord Herniation Inclusion Body Myositis Isolated Hyperckemia Lambert-Eaton Myasthenic Syndrome Lateral Sclerosis Leber Congenital Amaurosis 4 Limb-Girdle Muscular Dystrophy Lung Cancer Macrocephaly/megalencephaly Syndrome, Autosomal Recessive Major Affective Disorder 2 Mcleod Syndrome Megalencephaly Melanoma Microcephaly Multicentric Reticulohistiocytosis Multiple Sclerosis Muscle Tissue Disease Muscular Atrophy Muscular Dystrophy Muscular Dystrophy, Duchenne Type Muscular Dystrophy, Limb-Girdle, Type 2a Muscular Dystrophy, Limb-Girdle, Type 2b Muscular Dystrophy, Limb-Girdle, Type 2c Muscular Dystrophy, Limb-Girdle, Type 2f Myasthenia Gravis Myofibrillar Myopathy Myopathy Myositis Myotonia Myotonia Congenita Myotonic Dystrophy Necrotizing Autoimmune Myopathy Nemaline Myopathy Nemaline Myopathy 3 Neonatal Myasthenia Gravis Neuroblastoma Neuromuscular Disease Neuronitis Neuropathy Oculopharyngeal Muscular Dystrophy Osteomalacia Paresthesia Periodic Paralyses Poliomyelitis Polymyositis Polyneuropathy Progressive External Ophthalmoplegia with Mitochondrial Dna Deletions, Autosomal Dominant 2 Progressive External Ophthalmoplegia with Mitochondrial Dna Deletions, Autosomal Dominant 3 Progressive External Ophthalmoplegia with Mitochondrial Dna Deletions, Autosomal Dominant 4 Ptosis Renal Tubular Acidosis Retinitis Retinitis Pigmentosa Rheumatoid Arthritis Sarcoidosis 2 Scoliosis Small Cell Carcinoma Small Cell Carcinoma of the Bladder Spastic Cerebral Palsy Spasticity Spinal Muscular Atrophy Spinal Muscular Atrophy, Type Iii Spondylolisthesis Tay-Sachs Disease Tetanus Tethered Cord Syndrome Tetraamelia Syndrome, Autosomal Recessive Tick Paralysis Tooth Disease Trichorhinophalangeal Syndrome Trichorhinophalangeal Syndrome, Type Ii West Nile Encephalitis