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- Krankheit (de)
- σύνδρομο (el)
- хвороба (uk)
- مرض يصيب الإنسان (ar)
- 人类疾病 (zh)
- genetisk sjukdom (sv)
- affection rare, qui associe un hypogonadisme par insuffisance en hormones gonadotropes hypophysaires et un déficit de la perception des odeurs (fr)
- condizione genetica caratterizzata da ipogonadismo ipogonadotropo e da anosmia o disosmia (it)
- ଏହି ରୋଗରେ ଆଘ୍ରାଣହାନୀ ଏବଂ ଯୌନ ଅଭାବ ହୋଇଥାଏ । (or)
- תסמונת גנטית, המאופיינת בהיעדר בגרות מינית ופגיעה מלאה או חלקית בחוש הריח (iw)
- синдром фертильного евнуха (ru)
- form of hypogonadotropic hypogonadism which is also accompanied by a total lack or partial loss in the sense of smell. The condition affects people with XX or XY chromosomes and causes atypical puberty and infertility (en)
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- Richard von Krafft-Ebing, Charles Gilbert Chaddock (en)
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- 253.400000 (xsd:double)
- (en)
- E23.0 (en)
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- Absent or delayed puberty, infertility, inability to smell (en)
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- Kallmann's hereditary anosmia (en)
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- A case mentioned by Heschl [...] is remarkable, where the absence of both olfactory lobes was accompanied by imperfectly developed genitals. It was the case of a man aged 45, in all respects well developed, with the exception of the testicles, which were not larger than beans and contained no seminal canals, and the larynx, which seemed to be of feminine dimensions. Every trace of olfactory nerves was wanting, and the trigona olfactoria and the furrow on the under surface of the anterior lobes were absent. The perforations of the ethmoid plate were sparingly present, and occupied by nerveless processes of the dura instead of by nerves. In the mucous membrane of the nose there was also an absence of nerves. (en)
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- Kallmann syndrome (en)
- Σύνδρομο Κάλμαν (el)
- متلازمة كالمان (ar)
- Síndrome de Kallman (es)
- Kallmann-Syndrom (de)
- Syndrome de Kallmann (fr)
- Sindrome di Kallmann (it)
- 칼만 증후군 (ko)
- カルマン症候群 (ja)
- Zespół Kallmanna (pl)
- Síndrome de Kallmann (pt)
- Syndroom van Kallmann (nl)
- Kallmanns syndrom (sv)
- Синдром Каллмана (ru)
- 卡门氏症候群 (zh)
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