46,XY disorder of sex development due to isolated 17, 20 lyase deficiency (Q91110)
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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 |
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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. |
