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bn:06007118n
Noun Concept
NL
No term available
EN
genetic disease that has material basis in extra, missing, or re-arranged chromosomes Wikidata
Relations
Sources
IS A
ziekte
erfelijke aandoening
HAS KIND
syndroom van Down
syndroom van Klinefelter
Triple X-syndroom
syndroom van Angelman
syndroom van Russell-Silver
+7 relations
HAS INSTANCE
48, XXXX
EN
pentasomy X
HAS CAUSE
chromosomale afwijking
pathologie
HEALTH SPECIALTY
medische genetica

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