Congenital Hypogonadotropic Hypogonadism

Preferred Label : Congenital Hypogonadotropic Hypogonadism;

NCIt definition : Insufficient production of estrogen or testosterone in the ovaries or testes due to decreased secretion of gonadotropins as a result of pituitary or hypothalamus gland dysfunction that is present at birth.;

Alternative definition : NICHD: Hypogonadotropic hypogonadism, the cause of which is present at birth.;

Details

Origin ID

C120162;

UMLS CUI

C3899503;

Automatic exact mappings (from CISMeF team)
- Congenital hypogonadotropic hypogonadism [MedDRA Preferred Term]
Currated CISMeF NLP mapping
- Congenital hypogonadotropic hypogonadism [ORDO Disease]
- Congenital hypogonadotropic hypogonadism [Vue CIM-11]
- Congenital hypogonadotropic hypogonadism (disorder) [SNOMED CT concept]
Has associated anatomic sites
- Genitourinary System [NCIt concept]
- Gonad [NCIt concept]
- Reproductive System [NCIt concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Congenital hypogonadotropic hypogonadism [Vue CIM-11]
- Congenital hypogonadotropic hypogonadism [ORDO Disease]
- Congenital hypogonadotropic hypogonadism [MedDRA Preferred Term]
- Congenital hypogonadotropic hypogonadism (disorder) [SNOMED CT concept]
concept_is_in_subset
- NICHD Terminology [NCIt concept]
- Pediatric Endocrinology Terminology [NCIt concept]
disease_has_primary_anatomic_site
- Genitourinary System [NCIt concept]
- Gonad [NCIt concept]
- Reproductive System [NCIt concept]

Keyword's position in hierarchy(ies) :

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