Klinefelter syndrome
Term · Chemistry · MLC-T-CHM-006366
A genetic condition in males characterized by the presence of an extra X chromosome, resulting in a 47, XXY karyotype. This chromosomal abnormality leads to hypogonadism, reduced fertility, and often affects physical and cognitive development. It is one of the most common sex chromosome disorders in humans.
| Identifier | MLC-T-CHM-006366 |
|---|---|
| Field | Chemistry |
| Subject | Chemistry and Human Health |
| References | PAC, 2016, 88, 713. 'Glossary of terms used in developmental and reproductive toxicology (IUPAC Recommendations 2016)' on page 771 (https://doi.org/10.1515/pac-2015-1202) |
| See also | Syndrome; X chromosome; Spermatozoon; Testis |
Record as JSON
{
"id": "MLC-T-CHM-006366",
"term": "Klinefelter syndrome",
"field": "Chemistry",
"definition": "A genetic condition in males characterized by the presence of an extra X chromosome, resulting in a 47, XXY karyotype. This chromosomal abnormality leads to hypogonadism, reduced fertility, and often affects physical and cognitive development. It is one of the most common sex chromosome disorders in humans.",
"subject": "Chemistry and Human Health",
"see_also": [
"syndrome",
"X chromosome",
"spermatozoon",
"testis"
],
"references": [
"PAC, 2016, 88, 713. 'Glossary of terms used in developmental and reproductive toxicology (IUPAC Recommendations 2016)' on page 771 (https://doi.org/10.1515/pac-2015-1202)"
],
"url": "https://mlchart.com/terminology/chemistry/klinefelter-syndrome/"
}
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