loading...| Preferred Name | congenital hypogonadotropic hypogonadism | |
| Synonyms | ||
| Definitions |
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). |
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| ID |
http://purl.obolibrary.org/obo/MONDO_0015770 |
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| database_cross_reference |
UMLS:C3899503 NCIT:C120162 ICD10CM:E23.0 SCTID:722944006 NANDO:1200383 MEDGEN:859097 GARD:20135 icd11.foundation:1752075408 Orphanet:174590 |
|
| 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). |
|
| id |
MONDO:0015770 |
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| in_subset |
http://purl.obolibrary.org/obo/mondo/mondo-simple#otar http://purl.obolibrary.org/obo/mondo/mondo-simple#ordo_group_of_disorders http://purl.obolibrary.org/obo/mondo/mondo-simple#rare http://purl.obolibrary.org/obo/mondo/mondo-simple#disease_grouping |
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| label |
congenital hypogonadotropic hypogonadism |
|
| notation |
MONDO:0015770 |
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| prefLabel |
congenital hypogonadotropic hypogonadism |
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| skos_exactMatch |
http://purl.obolibrary.org/obo/Orphanet_174590 http://purl.obolibrary.org/obo/NCIT_C120162 http://identifiers.org/medgen/859097 http://linkedlifedata.com/resource/umls/id/C3899503 http://purl.obolibrary.org/obo/mondo/sources/icd11foundation/1752075408 |
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| treeView | ||
| subClassOf |