Matches in SemOpenAlex for { <https://semopenalex.org/concept/C2777280662> ?p ?o ?g. }
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- C2777280662 created "2018-01-05" @default.
- C2777280662 modified "2023-10-18" @default.
- C2777280662 type Concept @default.
- C2777280662 seeAlso "https://en.wikipedia.org/wiki/Lafora%20disease" @default.
- C2777280662 sameAs Q163905 @default.
- C2777280662 sameAs 2777280662 @default.
- C2777280662 broader C11960822 @default.
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- C2777280662 broader C55493867 @default.
- C2777280662 broader C86803240 @default.
- C2777280662 broader C95444343 @default.
- C2777280662 inScheme concepts @default.
- C2777280662 note "Lafora disease (LD) is a rare, inherited, severe, progressive myoclonic epilepsy characterized by myoclonus and/or generalized seizures, visual hallucinations (partial occipital seizures), and progressive neurological decline" @default.
- C2777280662 prefLabel "Lafora disease" @default.
- C2777280662 related C2775858608 @default.
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- C2777280662 citedByCount "18780" @default.
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- C2777280662 level "4" @default.
- C2777280662 magId "2777280662" @default.
- C2777280662 umlsCui "C0751783" @default.
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