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bn:26682202n
Noun Concept
JA
No term available
EN
monogenic disease that is has material basis in a mutation in a single gene on one of the non-sex chromosomes Wikidata
Relations
Sources
IS A
病気
EN
monogenic disease
HAS KIND
ハッチンソン・ギルフォード・プロジェリア症候群
EN
Gillespie syndrome
EN
hypophosphatasia
ソトス症候群
家族性地中海熱
+4 relations

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