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bn:02868430n
Noun Concept
SYL
No term available
EN
46,XX/46,XY is a chimeric genetic condition characterized by the presence of some cells that express a 46,XX karyotype and some cells that express a 46,XY karyotype in a single human being. Wikipedia
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IS A
EN
hermaphrodite
EN
rare disease
EN
Sex chromosome anomalies
EN
chimera

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