46,XY disorder of sex development due to isolated 17, 20 lyase deficiency (Q91110): Difference between revisions
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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.
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| default for all languages | ID_513865687 |
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| 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. |
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CID11:ID_513865687
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dki-india-ID_513865687
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