46,XY disorder of sex development due to 17-beta-hydroxysteroid dehydrogenase 3 deficiency (Q91106): Difference between revisions
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Deficiência da isozima 3 da 17-beta-hidroxiesteroide desidrogenase é um transtorno raro que leva a pseudo-hermafroditismo masculino, uma condição caracterizada por diferenciação incompleta da genitália masculina em homens 46X, Y. | |||
| description / en | description / en | ||
17-beta-hydroxysteroid dehydrogenase isozyme 3 deficiency is a rare disorder leading to male pseudohermaphroditism, a condition characterised by incomplete differentiation of the male genitalia in 46X,Y males. | |||
Revision as of 18:06, 15 August 2026
17-beta-hydroxysteroid dehydrogenase isozyme 3 deficiency is a rare disorder leading to male pseudohermaphroditism, a condition characterised by incomplete differentiation of the male genitalia in 46X,Y males.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_887793448 |
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| English | 46,XY disorder of sex development due to 17-beta-hydroxysteroid dehydrogenase 3 deficiency |
17-beta-hydroxysteroid dehydrogenase isozyme 3 deficiency is a rare disorder leading to male pseudohermaphroditism, a condition characterised by incomplete differentiation of the male genitalia in 46X,Y males. |
