eunuchoidism, familial hypogonadotropic

Preferred Label : eunuchoidism, familial hypogonadotropic;

MeSH synonym : gonadotropin deficiency, familial idiopathic;

Origin ID

C535764;

UMLS CUI

C1856897;

Automatic exact mappings (from CISMeF team)
- Hypogonadotropic hypogonadism 12 with or without anosmia [OMIM Phenotype]
Currated CISMeF NLP mapping
- Eunuchoidism, familial hypogonadotropic [OMIM Phenotype]
MeSH term(s) associated for indexing
- eunuchism [MeSH Descriptor]
Record concept(s)
- Eunuchoidism, familial hypogonadotropic [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Eunuchoidism, familial hypogonadotropic [OMIM Phenotype]
- Hypogonadotropic hypogonadism 12 with or without anosmia [OMIM Phenotype]
- hypogonadotropic hypogonadism 12 with or without anosmia [DO Concept]