hypogonadotropic hypogonadism

Preferred Label : hypogonadotropic hypogonadism;

UMLS semantic type : T047 - Disease or Syndrome;

Origin ID

M0472162;

UMLS CUI

C0271623;

Automatic exact mappings (from CISMeF team)
- Gonadotrophin deficiency [MedDRA Preferred Term]
- Gonadotropin deficiency [ICD-11 Subcategory]
- Hemochromatosis, type 1 [OMIM Phenotype]
- Hypopituitarism [ICD-10 Sub-category]
- Hypopituitarism [ICD-10 Sub-category (who)]
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 [SNOMED Notion]
Related record
- hypogonadism [MeSH Descriptor]
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 [SNOMED Notion]