Kallmann syndrome (Q1165179)
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A 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.
- Hypogonadism with anosmia (disorder)
- Kallman syndrome
- Kallman's syndrome
- Familial hypogonadism with anosmia
- GnRH deficiency
- Hypogonadism with anosmia
- de Morsier-Kallman's syndrome
- de Morsier's syndrome
- Hypogonadotropic hypogonadism
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | Kallmann syndrome |
A 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. |
|
Statements
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Kallmann syndrome
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Identifiers
Kallmann Syndrome
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2 February 2022
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Wikipedia(21 entries)
- arwiki متلازمة كالمان
- dewiki Kallmann-Syndrom
- elwiki Σύνδρομο Κάλμαν
- enwiki Kallmann syndrome
- eswiki Síndrome de Kallman
- fawiki سندرم کالمن
- fiwiki Kallmannin oireyhtymä
- frwiki Syndrome de Kallmann
- hewiki תסמונת קלמן
- itwiki Sindrome di Kallmann
- jawiki カルマン症候群
- kowiki 칼만 증후군
- nlwiki Syndroom van Kallmann
- orwiki କାଲମ୍ୟାନ ସିଣ୍ଡ୍ରୋମ
- plwiki Zespół Kallmanna
- ptwiki Síndrome de Kallmann
- ruwiki Синдром Каллмана
- srwiki Калманов синдром
- svwiki Kallmanns syndrom
- trwiki Kallmann sendromu
- zhwiki 卡门氏症候群
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Wiktionary(0 entries)
Multilingual sites(1 entry)
- commonswiki Category:Kallmann syndrome