46,XY disorder of sex development due to isolated 17, 20 lyase deficiency (Q91110): Difference between revisions

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+https://id.who.int/icd/entity/513865687
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+August 2026Timestamp +2026-08-13T00:00:00Z
Timezone +00:00
Calendar Gregorian
Precision 1 day
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After 0
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++2026-08-13T00:00:00Z
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@@ Property / Collection date: 13 August 2026 / rank @@
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Latest revision as of 18:06, 15 August 2026

This refers to disorder of sex development due to a rare endocrine and autosomal recessive genetic disorder which is characterised by a complete or partial loss of 17,20-lyase activity and, in turn, impaired production of the androgen and estrogen sex steroids.

Language	Label	Description	Also known as
default for all languages	ID_513865687
English	46,XY disorder of sex development due to isolated 17, 20 lyase deficiency	This refers to disorder of sex development due to a rare endocrine and autosomal recessive genetic disorder which is characterised by a complete or partial loss of 17,20-lyase activity and, in turn, impaired production of the androgen and estrogen sex steroids.