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Malattia rara
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Disgenesia gonadica completa 46,XY
Disgenesia gonadica completa 46,XY
ORPHA:
242
· ICD-10
Q99.1
· 46,XY complete gonadal dysgenesis
Prevalenza
Unknown
Trasmissione
Autosomal dominant, Autosomal recessive, X-linked recessive, Y-linked
Età di esordio
Adolescent, Adult
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