Male with 46,XX karyotype (Q46771): Difference between revisions
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Revision as of 15:34, 13 August 2026
A disease affecting males, characterised by hypergonadotropic hypogonadism, testosterone deficiency, and infertility. This condition may also present with hypospadias. This disease may be associated with abnormal crossing over of the sex chromosomes during meiosis in the father, resulting in the SRY gene being present on one or both copies of the X chromosome.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | LD52.0 |
||
| English | Male with 46,XX karyotype |
A disease affecting males, characterised by hypergonadotropic hypogonadism, testosterone deficiency, and infertility. This condition may also present with hypospadias. This disease may be associated with abnormal crossing over of the sex chromosomes during meiosis in the father, resulting in the SRY gene being present on one or both copies of the X chromosome. |
Statements
CID11:LD52.0
0 references
