46,XX testicular disorder of sex development (Q100830): Difference between revisions
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Cariótipo 46XX majoritariamente associado à recombinação anormal entre os cromossomos X e Y (transferência de SRY do cromossomo Y para o X); testículo sexual gonadal; fenótipo masculino. | |||
| description / en | description / en | ||
Karyotype 46XX mostly associated with abnormal recombination between X and Y chromosomes (transfer of SRY from Y to X chromosome) ; gonadal sex testis; male phenotype | |||
Revision as of 17:36, 16 August 2026
Karyotype 46XX mostly associated with abnormal recombination between X and Y chromosomes (transfer of SRY from Y to X chromosome) ; gonadal sex testis; male phenotype
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_1357942532 |
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| English | 46,XX testicular disorder of sex development |
Karyotype 46XX mostly associated with abnormal recombination between X and Y chromosomes (transfer of SRY from Y to X chromosome) ; gonadal sex testis; male phenotype |
