Informaţii despre

Nume Chronic Progressive External Ophthalmoplegia
Pagina Web www.malacards.org
Clasificare globală Malacards Boli metabolice; Boli rare
Clasificari ICD10 Progressive external ophthalmoplegia
Clasificare anatomică Malacards Boli ale ochiului; Boli musculare; Boli neuronale
Boli din aceeaşi familie Autosomal Dominant Progressive External Ophthalmoplegia

Vezi şi

Boli A-Z 3-Methylglutaconic Aciduria, Type V Aging Al-Raqad Syndrome Aniridia 1 Anorexia Nervosa 1 Arthrochalasia Ehlers-Danlos Syndrome Arthrogryposis, Renal Dysfunction, and Cholestasis 1 Ataxia and Polyneuropathy, Adult-Onset Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus Ataxia Neuropathy Spectrum Atrioventricular Block Autosomal Dominant Progressive External Ophthalmoplegia Axonal Neuropathy Blood Group--Ahonen Blood Group, I System Diabetic Polyneuropathy Dysphagia Encephalomyopathy Encephalopathy Exophthalmos Focal Segmental Glomerulosclerosis Hepatic Adenomas, Familial Hereditary Ataxia Hereditary Sensory Neuropathy Huntington Disease Hydrops, Lactic Acidosis, and Sideroblastic Anemia Hypercholesterolemia, Autosomal Dominant, 3 Hypogonadism Ichthyosis Intracranial Hypotension Kearns-Sayre Syndrome Keratopathy Lissencephaly 1 Lymphoma Maternally-Inherited Progressive External Ophthalmoplegia Mitochondrial Disorders Mitochondrial Dna-Associated Leigh Syndrome and Narp Mitochondrial Dna Depletion Syndrome 1 Mitochondrial Dna Depletion Syndrome 4a Mitochondrial Dna Depletion Syndrome 7 Mitochondrial Metabolism Disease Mitochondrial Myopathy Mitochondrial Neurogastrointestinal Encephalomyopathy Mitochondrial Neurogastrointestinal Encephalopathy Disease Motor Neuron Disease Multiple Mitochondrial Dysfunctions Syndrome 5 Multiple Sclerosis Muscular Dystrophy Myoclonic Epilepsy Associated with Ragged-Red Fibers Myoclonus Myopathy Nemaline Myopathy Neonatal Period Electroclinical Syndrome Neuronitis Neuropathy Ocular Motility Disease Oculopharyngeal Muscular Dystrophy Paralytic Ileus Paralytic Squint Pearson Marrow-Pancreas Syndrome Pharyngitis Polyglucosan Body Myopathy 1 with or Without Immunodeficiency Progressive External Ophthalmoplegia with Mitochondrial Dna Deletions, Autosomal Dominant 1 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 Progressive External Ophthalmoplegia with Mitochondrial Dna Deletions, Autosomal Recessive 1 Ptosis Retinitis Sensorineural Hearing Loss Sensory Ataxic Neuropathy, Dysarthria, and Ophthalmoparesis Spastic Paraplegia 7, Autosomal Recessive Strabismus Third-Degree Atrioventricular Block Total Internal Ophthalmoplegia Tremor Undifferentiated Pleomorphic Sarcoma