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Concept information

disease > metabolic diseases > mitochondrial myopathy > MELAS syndrome
disease > congenital disease > mitochondrial myopathy > MELAS syndrome
disease > striated muscle disease > myopathy > mitochondrial myopathy > MELAS syndrome
disease > enzymopathy > mitochondrial myopathy > MELAS syndrome
disease > nervous system diseases > mitochondrial myopathy > MELAS syndrome
... > disease > genetic disease > hereditary disease > mitochondrial disease > mitochondrial encephalopathy > MELAS syndrome
disease > enzymopathy > mitochondrial disease > mitochondrial encephalopathy > MELAS syndrome
... > disease > nervous system diseases > central nervous system diseases > cerebral disorder > encephalopathy > mitochondrial encephalopathy > MELAS syndrome
disease > metabolic disorder > acid-base balance disorder > acidosis > MELAS syndrome
... > disease > nervous system diseases > central nervous system diseases > cerebral disorder > cerebrovascular disease > stroke > MELAS syndrome
... > disease > cardiovascular disease > vascular disease > cerebrovascular disease > stroke > MELAS syndrome

Terme préférentiel

MELAS syndrome  

Définition

  • Mitochondrial encephalopathy, lactic acidosis, and stroke-like episodes (MELAS) is one of the family of mitochondrial cytopathies, which also include MERRF, and Leber's hereditary optic neuropathy. (Wikipedia)

Concept générique

Traductions

URI

http://data.loterre.fr/ark:/67375/VH8-TCTKRTDR-3

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