A mitochondrial encephalomyopathy that is characterized by mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes, has_symptom myalgia, motor weakness, headaches, seizures, and stroke-like episodes with acute hemiparesis and severe headaches, and develops_from mutation in mitochondrial genes including MT-TL1, which encodes tRNA proteins. [ url:https://ghr.nlm.nih.gov/condition/mitochondrial-encephalomyopathy-lactic-acidosis-and-stroke-like-episodes#genes http://purl.obolibrary.org/obo/ECO_0007637 ]
Synonyms: MITOCHONDRIAL MYOPATHY, ENCEPHALOPATHY, LACTIC ACIDOSIS, AND STROKE-LIKE EPISODES
Term information
- ICD10CM:E88.41
- MIM:540000
- NCI:C84885
- SNOMEDCT_US_2023_03_01:39925003
- MESH:D017241
- UMLS_CUI:C0162671
NCIthesaurus
Term relations
- mitochondrial encephalomyopathy
- has symptom some motor weakness
- has symptom some hemiparesis
- has symptom some seizure
- has symptom some severe headache
- has symptom some headache