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bn:14512446n
Noun Concept
EL
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
ασθένεια
HAS KIND
abetalipoproteinemia
κυστική ίνωση
συγγενή afibrinogenemia
δρεπανοκυτταρική νόσος
εκτροδακτυλία
+259 relations
HAS INSTANCE
τριμεθυλαμινουρία
HAS CAUSE
αυτοσωματικό κυρίαρχο
MODE OF INHERITANCE
αυτοσωματικό κυρίαρχο

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