Pseudohermaphroditism

  • Pseudohermaphroditism - Q56.3 Pseudohermaphroditism, unspecified
    • adrenal - E25.8 Other adrenogenital disorders
    • female - Q56.2 Female pseudohermaphroditism, not elsewhere classified
      • adrenal (congenital) - E25.0 Congenital adrenogenital disorders associated with enzyme deficiency
      • unspecified - E25.9 Adrenogenital disorder, unspecified
      • with adrenocortical disorder - E25.8 Other adrenogenital disorders
      • without adrenocortical disorder - Q56.2 Female pseudohermaphroditism, not elsewhere classified
    • male - Q56.1 Male pseudohermaphroditism, not elsewhere classified
      • adrenal - E25.8 Other adrenogenital disorders
      • unspecified - E25.9 Adrenogenital disorder, unspecified
      • with
        • 5-alpha-reductase deficiency - E29.1 Testicular hypofunction
        • adrenocortical disorder - E25.8 Other adrenogenital disorders
        • androgen resistance - E34.51 Complete androgen insensitivity syndrome
        • cleft scrotum - Q56.1 Male pseudohermaphroditism, not elsewhere classified
        • feminizing testis - E34.51 Complete androgen insensitivity syndrome
      • without gonadal disorder - Q56.1 Male pseudohermaphroditism, not elsewhere classified

Footnotes

Female:

Male:

Disorders of Sex Development: In gonochoristic organisms, congenital conditions in which development of chromosomal, gonadal, or anatomical sex is atypical. Effects from exposure to abnormal levels of GONADAL HORMONES in the maternal environment, or disruption of the function of those hormones by ENDOCRINE DISRUPTORS are included.