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bn:14512446n
Noun Concept
JA
No term available
EN
genetic disease characterized by the presence of two mutated copies of the gene, both of which must be present in order for the disease or trait to develop Wikidata
Relations
Sources
IS A
病気
HAS KIND
無β・リポタンパク血症
嚢胞性線維症
無フィブリノゲン血症
鎌状赤血球症
欠指
+259 relations
HAS INSTANCE
トリメチルアミン尿症
HAS CAUSE
優性
MODE OF INHERITANCE
優性

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