Term info
- ICD10CM:E23.0 (Orphanet:432/ntbt)
- ICD9:253.4 (MONDO:relatedTo)
- SCTID:33927004 (MONDO:equivalentTo)
- DOID:0090070 (MONDO:equivalentTo)
- OMIMPS:147950 (MONDO:equivalentTo)
- DOID:7455 (MONDO:equivalentObsolete)
- HP:0000044 (MONDO:otherHierarchy)
- UMLS:CN235466 (MONDO:equivalentTo)
- NCIT:C113347 (MONDO:equivalentTo)
- Orphanet:432 (MONDO:equivalentTo)
ordo_disease
Abnormal ovarian or testicular function due to insufficient hormonal stimulation from the hypothalamic-pituitary axis.
http://purl.obolibrary.org/obo/Orphanet_432, http://purl.obolibrary.org/obo/DOID_0090070, http://identifiers.org/snomedct/33927004, https://omim.org/phenotypicSeries/PS147950, http://purl.obolibrary.org/obo/NCIT_C113347, http://linkedlifedata.com/resource/umls/id/CN235466
secondary hypogonadism, gonadotropic deficiency, hypogonadotropic hypogonadism with or without anosmia, low gonadotropins (secondary hypogonadism), normosmic congenital hypogonadotropic hypogonadism, nIHH, Normosmic idiopathic hypogonadotropic hypogonadism, hypogonadism, hypogonadotropic, central hypogonadism, hypogonadotropic hypogonadism
congenital idiopathic hypogonadotropic hypogonadism, isolated congenital gonadotropin deficiency
hypogonadotropism, isolated hypogonadotropic hypogonadism
MONDO:0018555