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bn:14512446n
Noun Concept
NL
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
ziekte
HAS KIND
Abetalipoproteinemia
taaislijmziekte
aangeboren afibrinogenemia
sikkelcelanemie
ectrodactylie
+259 relations
HAS INSTANCE
visgeursyndroom
HAS CAUSE
dominantie
MODE OF INHERITANCE
dominantie

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