Informaţii despre

Nume Mitochondrial Myopathy
Pagina Web www.malacards.org
Clasificare globală Malacards Boli metabolice; Boli rare
Clasificare anatomică Malacards Boli musculare; Boli neuronale
Boli din aceeaşi familie Mitochondrial Myopathy, Infantile, Transient

Vezi şi

Boli A-Z Aging Alexia Alopecia, Neurologic Defects, and Endocrinopathy Syndrome Al-Raqad Syndrome Aniridia 1 Anorexia Nervosa 1 Arthrochalasia Ehlers-Danlos Syndrome Ataxia and Polyneuropathy, Adult-Onset Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus Autism Autosomal Dominant Progressive External Ophthalmoplegia Blood Group--Ahonen Blood Group, I System Branchiootic Syndrome 1 Cardiac Tamponade Carrion's Disease Cataract Cervicitis Chronic Fatigue Syndrome Chronic Inflammatory Demyelinating Polyneuropathy Chronic Progressive External Ophthalmoplegia Coenzyme Q10 Deficiency Disease Cortical Blindness Deafness, Aminoglycoside-Induced Deafness, Nonsyndromic Sensorineural, Mitochondrial Dementia Demyelinating Polyneuropathy Deoxyguanosine Kinase Deficiency Diabetes Mellitus Dihydrolipoamide Dehydrogenase Deficiency Dysautonomia Encephalomyopathy Encephalopathy Epilepsy Fabry Disease Fanconi Syndrome Glycogen Storage Disease Glycogen Storage Disease V Growth Hormone Deficiency Headache Hereditary Hearing Loss and Deafness Hereditary Neuropathies Hydrops, Lactic Acidosis, and Sideroblastic Anemia Hypertrophic Cardiomyopathy Hypophosphatemia Hypotonia Infertility Inherited Metabolic Disorder Intestinal Pseudo-Obstruction Kearns-Sayre Syndrome Lactic Acidosis Leber Hereditary Optic Neuropathy Leber Optic Atrophy Leigh Syndrome Lipomatosis Lissencephaly 1 Lung Cancer Malignant Hyperthermia Malignant Hyperthermia Susceptibility Maternally-Inherited Progressive External Ophthalmoplegia Meningoencephalitis Mitochondrial Complex Iv Deficiency Mitochondrial Disorders Mitochondrial Dna-Associated Leigh Syndrome and Narp Mitochondrial Dna Depletion Syndrome 4a Mitochondrial Encephalomyopathy Mitochondrial Metabolism Disease Mitochondrial Myopathy, Encephalopathy, Lactic Acidosis, and Stroke-Like Episodes Mitochondrial Myopathy with Lactic Acidosis Mitochondrial Non-Syndromic Sensorineural Deafness Mohr-Tranebjaerg Syndrome Muir-Torre Syndrome Multiple Symmetrical Lipomatosis Muscular Dystrophy Myoclonic Epilepsy Associated with Ragged-Red Fibers Myoclonus Myoclonus Epilepsy Myopathy Myopathy, Lactic Acidosis, and Sideroblastic Anemia Myopathy, Lactic Acidosis, and Sideroblastic Anemia 1 Myopathy with Lactic Acidosis, Hereditary Myotonic Dystrophy Nail-Patella Syndrome Neuromuscular Disease Neuropathy Pearson Marrow-Pancreas Syndrome Pericarditis Pfeiffer Syndrome Polyneuropathy Primary Biliary Cirrhosis 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 Progressive Myoclonus Epilepsy Pure Mitochondrial Myopathy Retinitis Riboflavin Transporter Deficiency Sideroblastic Anemia Sparganosis Status Epilepticus Visceral Myopathy Yemenite Deaf-Blind Hypopigmentation Syndrome Zellweger Syndrome