SE-ATLAS

Septate vagina Mayer-Rokitansky-Küster-Hauser syndrome type 2 Complete androgen insensitivity syndrome True unicornuate uterus Bicervical bicornuate uterus and blind hemivagina Unicervical bicornuate uterus Complete septate uterus Mayer-Rokitansky-Küster-Hauser syndrome type 1 Partial septate uterus Partial androgen insensitivity syndrome Uterine hypoplasia Uterine cervical aplasia and agenesis Absence of uterine body Isolated partial vaginal agenesis Pseudounicornuate uterus 46,XX testicular difference of sex development 46,XX ovarian dysgenesis-short stature syndrome Bicervical bicornuate uterus with patent cervix and vagina 46,XX ovotesticular difference of sex development Hyperandrogenism due to cortisone reductase deficiency Generalized glucocorticoid resistance syndrome Congenital adrenal hyperplasia due to cytochrome P450 oxidoreductase deficiency Aromatase deficiency Müllerian aplasia and hyperandrogenism 46,XX difference of sex development-anorectal anomalies syndrome 46,XX difference of sex development-skeletal anomalies syndrome 45,X/46,XY mixed gonadal dysgenesis 46,XX gonadal dysgenesis Mayer-Rokitansky-Küster-Hauser syndrome Adrenogenital syndrome Congenital adrenal hyperplasia due to 3-beta-hydroxysteroid dehydrogenase deficiency Nebennierenhyperplasie, kongenitale lipoide, durch STAR-Mangel Nebennierenhyperplasie, kongenitale, durch 17-alpha-Hydroxylase-Mangel Nebennierenhyperplasie, kongenitale, durch 11-beta-Hydroxylase-Mangel Nebennierenhyperplasie, kongenitale, durch 21-Hydroxylase-Mangel, klassische Form 46,XY-Gonadendysgenesie, partielle Störung der Geschlechtsentwicklung 46,XY, durch isolierten 17,20-Lyase-Mangel Störung der Geschlechtsentwicklung 46,XY, durch 17-beta-Hydroxysteroid-Dehydrogenase 3-Mangel Störung der Geschlechtsentwicklung 46,XY, durch 5-Alpha-Reduktase 2-Mangel Tetragametischer Chimärismus 46,XY-Gonadendysgenesie, vollständige Uterus Didelphys