Eunuchoidism, familial hypogonadotropic

Preferred Label : Eunuchoidism, familial hypogonadotropic;

Obsolete resource : true;

Moved to : 614841;

Alternative titles and symbols : Gonadotropin deficiency, familial idiopathic; Figd;

Inheritance : Autosomal recessive;

Prefixed ID : 227200;

Details

Origin ID

227200;

UMLS CUI

C1856897;

Currated CISMeF NLP mapping
- Eunuchoidism, familial hypogonadotropic [MeSH concept]
- eunuchoidism, familial hypogonadotropic [MeSH Supplementary Concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Eunuchoidism, familial hypogonadotropic [MeSH concept]
- eunuchoidism, familial hypogonadotropic [MeSH Supplementary Concept]
- hypogonadotropic hypogonadism 12 with or without anosmia [DO Concept]

Keyword's position in hierarchy(ies) :

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