SE-ATLAS

46,XX difference of sex development induced by fetal androgens excess Congenital urachal anomaly Penile agenesis Open spinal dysraphism Total spina bifida aperta Congenital primary megaureter Hinman syndrome Nephroblastoma Ochoa syndrome Fetal lower urinary tract obstruction Classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency Diphallia Congenital agenesis of the scrotum Penoscrotal transposition Turner syndrome Idiopathic isolated micropenis Duplication of urethra Spina bifida and other spinal dysraphisms Posterior urethral valve Total spina bifida cystica Caudal regression syndrome Non-syndromic posterior hypospadias Rhabdomyosarcoma Non-syndromic anorectal malformation with H-type fistula Exstrophy-epispadias complex Non-syndromic anorectal malformation with rectourethral fistula, prostatic type Non-syndromic anorectal malformation with rectourethral fistula Non-syndromic anorectal malformation with rectovaginal fistula Non-syndromic anorectal malformation with rectourethral fistula, bulbar type Non-syndromic anorectal malformation with rectovesical fistula Non-syndromic anorectal malformation without fistula 46,XY difference of sex development Cloacal exstrophy Non-syndromic anorectal malformation with vestibular fistula Bladder exstrophy Absence of uterine body Non-syndromic cloacal malformation Non-syndromic anorectal malformation with perineal fistula Non-syndromic anorectal malformation with rectal atresia Non-syndromic anorectal malformation with rectal stenosis VACTERL/VATER association Nicht-syndromale anorektale Fehlbildung mit Analstenose Nicht-syndromale anorektale Fehlbildung mit Pouch-Kolon