"Klinefelter syndrome" meaning in English

See Klinefelter syndrome in All languages combined, or Wiktionary

Noun

Etymology: Named after Harry Klinefelter, who identified the condition in the 1940s. Etymology templates: {{!}} |, {{lang|en|Harry Klinefelter}} Harry Klinefelter, {{named-after|en|Harry Klinefelter|wplink==}} Named after Harry Klinefelter Head templates: {{en-noun|-}} Klinefelter syndrome (uncountable)
  1. A genetic condition in which a person is born with two X chromosomes and one Y chromosome. Wikipedia link: Klinefelter syndrome Tags: uncountable Categories (topical): Intersex Translations (genetic condition): 克氏症候群 (Kèshì zhènghòuqún) (Chinese Mandarin), 克蘭費爾特症候群 (Chinese Mandarin), 克兰费尔特症候群 (kèlánfèi'ěrtè zhènghòuqún) (Chinese Mandarin), syndrome de Klinefelter (French), Klinefelter-Syndrom [neuter] (German), sindrom Klinefelter (Indonesian), クラインフェルター症候群 (Kurainferutā shōkōgun) (Japanese), sindrom Klinefelter (Malay), zespół Klinefeltera [masculine] (Polish), síndrome de Klinefelter [feminine] (Portuguese), síndrome de Klinefelter [masculine] (Spanish), Klinefelter sendromu (Turkish)

Alternative forms

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This page is a part of the kaikki.org machine-readable English dictionary. This dictionary is based on structured data extracted on 2024-12-21 from the enwiktionary dump dated 2024-12-04 using wiktextract (d8cb2f3 and 4e554ae). The data shown on this site has been post-processed and various details (e.g., extra categories) removed, some information disambiguated, and additional data merged from other sources. See the raw data download page for the unprocessed wiktextract data.

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