Informaţii despre

Nume Mitochondrial Myopathy, Encephalopathy, Lactic Acidosis, and Stroke-Like Episodes
Pagina Web www.malacards.org
Clasificare globală Malacards Boli fetale; Boli genetice; Boli metabolice; Boli rare
Clasificari ICD10 Mitochondrial myopathy, not elsewhere classified
Clasificare anatomică Malacards Boli ale ochiului; Boli ale urechii; Boli musculare; Boli neuronale

Vezi şi

Boli A-Z 3-Methylglutaconic Aciduria, Type V Aging Alport Syndrome, X-Linked Al-Raqad Syndrome Aniridia 1 Anorexia Nervosa 1 Arthrochalasia Ehlers-Danlos Syndrome Aspergillosis Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus Autism Blood Group--Ahonen Cercarial Dermatitis Cerebritis Chickenpox Chronic Progressive External Ophthalmoplegia Coenurosis Cortical Blindness Cortical Deafness Cranial Nerve Disease Cystadenocarcinoma Cystic Echinococcosis Deafness, Aminoglycoside-Induced Deafness, Nonsyndromic Sensorineural, Mitochondrial Dementia Diabetes and Deafness, Maternally Inherited Diabetes Mellitus Diphyllobothriasis Dysfibrinogenemia Echinococcosis Encephalitis Encephalomyopathy Encephalopathy Familial Colorectal Cancer Fanconi Syndrome Frontotemporal Lobar Degeneration with Tdp43 Inclusions, Grn-Related Genetic Recurrent Myoglobinuria Growth Hormone Deficiency Headache Hereditary Hearing Loss and Deafness Herpes Simplex Herpes Simplex Encephalitis Hyperglycemia Hyperthyroidism Intestinal Pseudo-Obstruction Invasive Aspergillosis Kearns-Sayre Syndrome Lactic Acidosis Leber Hereditary Optic Neuropathy Leber Optic Atrophy Leber Optic Atrophy and Dystonia Leigh Syndrome Maternally-Inherited Progressive External Ophthalmoplegia Meningoencephalitis Mitochondrial Complex Iv Deficiency Mitochondrial Disorders Mitochondrial Dna-Associated Leigh Syndrome and Narp Mitochondrial Dna Depletion Syndrome 1 Mitochondrial Dna Depletion Syndrome 4a Mitochondrial Encephalomyopathy Mitochondrial Metabolism Disease Mitochondrial Myopathy Mitochondrial Neurogastrointestinal Encephalomyopathy Mitochondrial Neurogastrointestinal Encephalopathy Disease Mitochondrial Non-Syndromic Sensorineural Deafness Moyamoya Disease 4 with Short Stature, Hypergonadotropic Hypogonadism, and Facial Dysmorphism Myasthenic Syndrome, Congenital, 10 Myiasis Myoclonic Epilepsy Associated with Ragged-Red Fibers Myopathy Myopathy, Lactic Acidosis, and Sideroblastic Anemia Nervous System Disease Neuronitis Neuropathy Neutrophil Actin Dysfunction Optic Nerve Disease Paralytic Ileus Parkinson Disease 6, Autosomal Recessive Early-Onset Pearson Marrow-Pancreas Syndrome Polyglucosan Body Myopathy 1 with or Without Immunodeficiency Pulmonary Embolism Retinitis Semantic Dementia Sensorineural Hearing Loss Sideroblastic Anemia Sparganosis Status Epilepticus Stroke, Ischemic Thyroiditis Yemenite Deaf-Blind Hypopigmentation Syndrome