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bn:05219062n
Noun Named Entity
NL
No term available
EN
Human disease Wikidata
Relations
Sources
IS A
erfelijke aandoening
HAS KIND
amyotrofische laterale sclerose
cataract
Hereditaire motorische en sensorische neuropathieën
EN
3C syndrome
Syndroom van Cornelia de Lange
+18 relations
HAS CAUSE
EN
single gene mutation
OPPOSITE OF
EN
polygenic disease

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