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bn:05219062n
Noun Named Entity
IT
No term available
EN
Human disease Wikidata
Relations
Sources
IS A
malattia genetica
HAS KIND
sclerosi laterale amiotrofica
cataratta
malattia di Charcot-Marie-Tooth
EN
3C syndrome
sindrome di Cornelia de Lange
+18 relations
HAS CAUSE
EN
single gene mutation
OPPOSITE OF
EN
polygenic disease

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