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LD2A.3 46,XY disorder of sex development due to a defect in testosterone metabolism

International Classification of Diseases for Mortality and Morbidity Statistics, 11th Revision, v2024-01

exclusions

• Congenital adrenal hyperplasia  (5A71.01)

code elsewhere

• Smith-Lemli-Opitz syndrome  (5C52.10)

synonyms

• 46,XY disorder of sex development due to a defect in testosterone metabolism
• 46,XY DSD due to a defect in testosterone metabolism
• 46,XY disorder of sex development due to 17-beta-hydroxysteroid dehydrogenase 3 deficiency
• Male pseudohermaphroditism due to 17-beta-hydroxysteroid dehydrogenase 3 deficiency
• 17-beta-hydroxysteroid dehydrogenase 3 deficiency
• 17-ketosteroidreductase deficiency
• 17-ketoreductase deficiency
• 46,XY DSD due to 17-beta-hydroxysteroid dehydrogenase 3 deficiency
• 46,XY disorder of sex development due to 5-alpha-reductase 2 deficiency
• 46,XY DSD due to 5-alpha-reductase 2 deficiency
• Male pseudohermaphroditism due to 5-alpha-reductase 2 deficiency
• 46,XY disorder of sex development due to isolated 17, 20 lyase deficiency
• 46,XY DSD due to isolated 17, 20 lyase deficiency
• Leydig cell hypoplasia
• 46,XY disorder of sex development due to LH defects
• LH resistance due to LH receptor inactivation
• 46,XY DSD due to LH defects
• Male pseudohermaphrodism due to LH defects
• LH resistance due to complete LH receptor inactivation
• LH resistance due to partial LH receptor inactivation

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