Mitochondrial Encephalomyopathy, Lactic Acidosis and Stroke Like Episodes (MELAS)
DBCOND0133949Congenital, Hereditary, and Neonatal Diseases and AbnormalitiesMusculoskeletal and Connective Tissue Diseases
Mitochondrial Encephalomyopathy, Lactic Acidosis and Stroke Like Episodes (MELAS) is a condition in DrugBank's curated disease hierarchy.
- Also known as
- MELAS Syndrome · Melas · Mitochondrial Encephalomyopathy, Lactic Acidosis, and Stroke-Like Episodes · Mitochondrial Encephalopathy, Lactic Acidosis and Stroke-Like Episodes (MELAS Syndrome) · Mitochondrial Encephalopathy (MELAS)
Resolves to
Vocabularies
What you can answer from here — as of September 30, 2026
Which drugs are in clinical trials for Mitochondrial Encephalomyopathy, Lactic Acidosis and Stroke Like Episodes (MELAS), in which phases, and against which targets?
Create a free account or log in to explore the full data card.
Create Account