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| Term | MELAS syndrome | ID (Ontology) | DOID:3687 (Human Disease) |
| Definition | 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. | ||
| Also Known As | "MITOCHONDRIAL MYOPATHY, ENCEPHALOPATHY, LACTIC ACIDOSIS, AND STROKE-LIKE EPISODES" | ||
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| DO.org | |||
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| Records annotated with this term OR any of its CHILD TERMS | |||
Full annotation statements including this term (annotations to child terms are NOT included), and relevant FlyBase records
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mitochondrial myopathy |__mitochondrial encephalomyopathy |__MELAS syndrome |
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| Is a | mitochondrial encephalomyopathy | ||
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External Crossreferences & Linkouts
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ICD10CM:E88.41 MESH:D017241 MIM:540000 NCI:C84885 SNOMEDCT_US_2023_03_01:39925003 UMLS_CUI:C0162671 |
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