Description of the disease * EnglishPolish Pobierz sekcję do PDF Definition A rare neurometabolic genetic disorder which is progressive and multisystemic due to mitochondrial dysfunction and that is characterized by encephalomyopathy, lactic acidosis, and stroke-like episodes. Disease data Classification Disease Synonyms Mitochondrial encephalomyopathy, lactic acidosis and stroke-like episodes Encefalopatia mitochondrialna, kwasica mleczanowa z epizodami udaropodobnymi Miopatia mitochondrialna, encefalopatia, kwasica mleczanowa i epizody udaropodobne Mitochondrial encephalopathy, lactic acidosis, and stroke-like episodes Mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes ORPHA code 550 OMIM code 540000 ICD10 code G71.3 ICD11 code 8C73.Y *Soruce Extended description of the disease Pobierz sekcję do PDF No additional description. Orphanet - interntowa baza danych dotyczących rzadkich chorób i sierochych leków. ©INSERM 1999 - Dostępna na stronie www.orphanet.pl