Hypogonadism, male

Preferred Label : Hypogonadism, male;

Obsolete resource : true;

Moved to : 312300;

Inheritance : X-linked; Also autosomal dominant (male-limited), and autosomal recessive (male-limited); Forms;

Prefixed ID : 307300;

Details

Origin ID

307300;

UMLS CUI

C0151721;

Automatic exact mappings (from CISMeF team)
- eunuchism [MeSH Descriptor]
Currated CISMeF NLP mapping
- Eunuchoidism [MedDRA Preferred Term]
- Hypogonadism male [MedDRA Preferred Term]
- Male hypogonadism [HPO term]
- Male hypogonadism (disorder) [SNOMED CT concept]
- male hypogonadism [Disease (Nov.)]
- male hypogonadism, nos [SNOMED Notion]
- male hypogonadism, nos [TUV Term]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Eunuchoidism [MedDRA Preferred Term]
- Hypogonadism male [MedDRA Preferred Term]
- Male hypogonadism [HPO term]
- Male hypogonadism (disorder) [SNOMED CT concept]
- Testicular Failure [NCIt concept]
- Testicular failure [MedDRA Preferred Term]
- Testicular failure NOS [MedDRA LLT]
- Testicular hypogonadism [MedDRA LLT]
- eunuchoidism [MeSH concept]
- eunuchoidism, nos [SNOMED Notion]
- male hypogonadism [Disease (Nov.)]
- male hypogonadism, nos [SNOMED Notion]
- testicular hypogonadism, nos [SNOMED Notion]

Keyword's position in hierarchy(ies) :

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