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Concept information

Endocrine System Diseases > Gonadal Disorders > Disorders of Sex Development > Ovotesticular Disorders of Sex Development
... > Urogenital Diseases > Female Urogenital Diseases and Pregnancy Complications > Female Urogenital Diseases > Urogenital Abnormalities > Disorders of Sex Development > Ovotesticular Disorders of Sex Development
Urogenital Diseases > Male Urogenital Diseases > Urogenital Abnormalities > Disorders of Sex Development > Ovotesticular Disorders of Sex Development
Congenital, Hereditary, and Neonatal Diseases and Abnormalities > Congenital Abnormalities > Urogenital Abnormalities > Disorders of Sex Development > Ovotesticular Disorders of Sex Development

Terme préférentiel

Ovotesticular Disorders of Sex Development  

Type

  • mesh:Descriptor

Définition

  • Conditions of sexual ambiguity in which the individual possesses gonadal tissues of both sexes, tissues from the OVARY and the TESTIS. There can be a testis on one side and an ovary on the other (lateral), or there may be combined ovarian and testicular tissue (ovotestes) on each side (bilateral). The karyotype may be 46,XX; 46,XY; or a mosaic of 46,XX/46,XY. These disorders have historically been called true hermaphroditism. An historical term for conditions of sexual ambiguity in which the individual possesses gonadal tissues of both sexes.

Concept générique

Synonyme(s)

  • 46,XX Gonadal Dysgenesis, Complete, Sry-Positive
  • 46,XX True Hermaphroditism, Sry-Positive
  • Ovotesticular Disorder Of Sex Development
  • Ovotesticular DSD
  • XX Male Syndrome, Sry-Positive

Qualificatif(s) autorisé(s)

Traductions

URI

http://data.loterre.fr/ark:/67375/JVR-JL50FCSN-J

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RDF/XML TURTLE JSON-LD Date de création 30/06/2005, dernière modification le 30/06/2021