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bn:14505700n
Noun Concept
EL
No term available
EN
Myhre syndrome is a rare genetic disorder inherited in an autosomal dominant fashion. Wikipedia
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Sources
IS A
ασθένεια
σπάνια πάθηση
EN
hereditary disorder
EN
multiple abnormalities
GENETIC ASSOCIATION
EN
mothers against decapentaplegic homolog 4

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