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congenital hypogonadotropic hypogonadism

^ http://purl.obolibrary.org/obo/MONDO_0015770

Congenital hypogonadotropic hypogonadism (CHH) is a rare disorder of sexual maturation characterized by gonadotropin (Gn) deficiency with low sex steroid levels associated with low levels of follicle stimulating hormone (FSH) and luteinizing hormone (LH). [ Orphanet:174590 ]

Term info

database cross reference
  • Orphanet:174590 (MONDO:equivalentTo)
  • SCTID:722944006 (MONDO:equivalentTo)
  • NCIT:C120162 (MONDO:equivalentTo)
  • ICD10CM:E23.0 (Orphanet:174590/ntbt)
  • UMLS:C3899503 (NCIT:C120162)
Subsets

disease_grouping, ordo_group_of_disorders

definition

Congenital hypogonadotropic hypogonadism (CHH) is a rare disorder of sexual maturation characterized by gonadotropin (Gn) deficiency with low sex steroid levels associated with low levels of follicle stimulating hormone (FSH) and luteinizing hormone (LH).

exactMatch

http://purl.obolibrary.org/obo/Orphanet_174590, http://purl.obolibrary.org/obo/NCIT_C120162, http://identifiers.org/snomedct/722944006, http://linkedlifedata.com/resource/umls/id/C3899503

id

MONDO:0015770