Klinefelter syndrome
English
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Klinefelter syndrome
Where it comes from
Named after Harry Klinefelter, who identified the condition in the 1940s.
noun
- A genetic condition in which a person is born with two X chromosomes and one Y chromosome.
Translations
Every language
noun genetic condition
| Español | síndrome de Klinefelter |
|---|---|
| 日本語 | クラインフェルター症候群 Kurainferutā shōkōgun |
| 中文 | 克氏症候群 Kèshì zhènghòuqún, 克蘭費爾特症候群 /克兰费尔特症候群 kèlánfèi'ěrtè zhènghòuqún |
| Português | síndrome de Klinefelter |
| Français | syndrome de Klinefelter |
| Deutsch | Klinefelter-Syndrom |
Talk about this word "Klinefelter syndrome." Wiktionary, via Micwyn, micwyn.com/word/klinefelter%20syndrome. Accessed 6 Nov. 2026. Klinefelter syndrome. (n.d.). In Wiktionary, via Micwyn. Retrieved November 6, 2026, from https://micwyn.com/word/klinefelter%20syndrome "Klinefelter syndrome." Wiktionary, via Micwyn. Accessed November 6, 2026. https://micwyn.com/word/klinefelter%20syndrome.Cite this
@misc{klinefelter_syndrome_2026,
title = {Klinefelter syndrome},
howpublished = {Wiktionary, via Micwyn},
year = {2026},
url = {https://micwyn.com/word/klinefelter%20syndrome},
urldate = {2026-11-06}
}