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congenital hypogonadotropic hypogonadism

Go to external page 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 ]

This is just here as a test because I lose it

Term information

database cross reference
  • UMLS:C3899503 (NCIT:C120162)
  • GARD:20135 (Orphanet:174590)
  • NCIT:C120162 (MONDO:equivalentTo)
  • SCTID:722944006 (MONDO:equivalentTo)
  • ICD10CM:E23.0 (Orphanet:174590/ntbt)
  • Orphanet:174590 (MONDO:equivalentTo)
Subsets

gard_rare, disease_grouping, rare, orphanet_rare, ordo_group_of_disorders

exactMatch

http://purl.obolibrary.org/obo/NCIT_C120162

http://identifiers.org/snomedct/722944006

http://www.orpha.net/ORDO/Orphanet_174590

http://linkedlifedata.com/resource/umls/id/C3899503

id

MONDO:0015770