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Nume Mitochondrial Encephalomyopathy
Pagina Web www.malacards.org
Clasificare anatomică Malacards Boli musculare

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Boli A-Z Acquired Idiopathic Sideroblastic Anemia Aging Amelogenesis Imperfecta, Type Iv Amenorrhea Aminoacidopathies 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 Atrioventricular Block Bleeding Disorder, Platelet-Type, 11 Blood Group--Ahonen Blood Group, I System Cataract Cercarial Dermatitis Cerebral Hemorrhage Cerebritis Choroiditis Chronic Progressive External Ophthalmoplegia Coenurosis Combined Oxidative Phosphorylation Deficiency 6 Cortical Blindness Cranial Nerve Disease Deafness, Aminoglycoside-Induced Deafness, Nonsyndromic Sensorineural, Mitochondrial Dementia Diabetes and Deafness, Maternally Inherited Diabetes Mellitus Diphyllobothriasis Early Myoclonic Encephalopathy Encephalitis Encephalomyopathy Endotheliitis Epilepsy Familial Colorectal Cancer Fanconi Syndrome Fatal Infantile Encephalocardiomyopathy Focal Segmental Glomerulosclerosis Fumarase Deficiency Genetic Recurrent Myoglobinuria Gonadal Disease Growth Hormone Deficiency Herpes Simplex Herpes Simplex Encephalitis Hypertrophic Cardiomyopathy Hypoparathyroidism Hypopituitarism Isolated Complex Iii Deficiency Kearns-Sayre Syndrome Lactic Acidosis Leber Hereditary Optic Neuropathy Leber Optic Atrophy Leber Optic Atrophy and Dystonia Leigh Syndrome Leukodystrophy Lice Infestation Lissencephaly 1 Maternally-Inherited Progressive External Ophthalmoplegia Mitochondrial Complex Iv Deficiency Mitochondrial Disorders Mitochondrial Dna-Associated Leigh Syndrome and Narp Mitochondrial Dna Depletion Syndrome 4a Mitochondrial Metabolism Disease Mitochondrial Myopathy Mitochondrial Myopathy, Encephalopathy, Lactic Acidosis, and Stroke-Like Episodes Muscular Dystrophy Mutism Myasthenic Syndrome, Congenital, 10 Myiasis Myoclonic Cerebellar Dyssynergia Myoclonic Epilepsy Associated with Ragged-Red Fibers Myoclonus Myoglobinuria Myoglobinuria, Recurrent Myotonic Dystrophy Open-Angle Glaucoma Optic Nerve Disease Pancreatitis Parkinson Disease 6, Autosomal Recessive Early-Onset Pearson Marrow-Pancreas Syndrome Polyhydramnios Retinal Detachment Retinitis Retinoblastoma Ring Chromosome 18 Sensorineural Hearing Loss Sleep Apnea Sparganosis Superior Mesenteric Artery Syndrome Taeniasis Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 6