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bn:22200452n
Noun Concept
ES
No term available
EN
The Emberger syndrome is a rare, autosomal dominant, genetic disorder caused by familial or sporadic inactivating mutations in one of the two parental GATA2 genes. Wikipedia
Relations
Sources
IS A
enfermedad
enfermedad rara
cáncer de cabeza y cuello
neoplasias hematológicas
GENETIC ASSOCIATION
GATA2

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