hypogonadotropic hypogonadism

Preferred Label : hypogonadotropic hypogonadism;

Détails

Origin ID

DB-12710;

UMLS CUI

C0271623;

Automatic exact mappings (from CISMeF team)
- Gonadotrophin deficiency [MedDRA Preferred Term]
- Gonadotropin deficiency [ICD-11 Subcategory]
- Hypopituitarism [ICD-10 Sub-category (who)]
- Secondary hypogenitalism [MedDRA LLT]
- hypogonadism [MeSH Descriptor]
Currated CISMeF NLP mapping
- Hypogonadotrophic hypogonadism [MedDRA LLT]
- Hypogonadotropic Hypogonadism [NCIt concept]
- Hypogonadotropic hypogonadism [PASCAL descriptor]
- Hypogonadotropic hypogonadism [HPO term]
- Hypogonadotropic hypogonadism (disorder) [SNOMED CT concept]
- Klinefelter Syndrome [NCIt concept]
- Klinefelter syndrome [DO Concept]
- Secondary hypogonadism [MedDRA Preferred Term]
- hypogonadotropic hypogonadism [DO Concept]
- hypogonadotropic hypogonadism [Disease (Nov.)]
- hypogonadotropic hypogonadism [MeSH concept]
Décrit
- hypogonadism with anosmia [SNOMED Notion]
ICD-10 exact mapping(s)
- Hypopituitarism [ICD-10 Sub-category (who)]
Metaterm(s)
- endocrinology [CISMeF Metaterm]
SNOMED CT concept
- Hypogonadotropic hypogonadism (disorder) [SNOMED CT concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Gonadotropin deficiency [HPO term]
- Hypogonadotrophic hypogonadism [MedDRA LLT]
- Hypogonadotropic Hypogonadism [NCIt concept]
- Hypogonadotropic hypogonadism [HPO term]
- Hypogonadotropic hypogonadism (disorder) [SNOMED CT concept]
- Rare disorder with multisystemic involvement and congenital hypogonadotropic hypogonadism [ORDO Disease]
- Secondary hypogonadism [MedDRA Preferred Term]
- hypogonadotropic hypogonadism [MeSH concept]
Validated automatic mappings to BTNT
- hypogonadism, isolated hypogonadotropic [MeSH concept]

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