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bn:14512446n
Noun Concept
SYL
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
EN
disease
HAS KIND
EN
abetalipoproteinemia
EN
cystic fibrosis
EN
congenital afibrinogenemia
EN
sickle-cell anemia
EN
ectrodactyly
+259 relations
HAS INSTANCE
EN
trimethylaminuria
HAS CAUSE
EN
dominance
MODE OF INHERITANCE
EN
dominance

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