Preferred Name |
congenital hypogonadotropic hypogonadism |
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Synonyms |
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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 GARD:20135 Orphanet:174590 |
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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). |
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exactMatch |
http://purl.obolibrary.org/obo/Orphanet_174590 http://purl.obolibrary.org/obo/NCIT_C120162 |
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id |
MONDO:0015770 |
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in_subset |
http://purl.obolibrary.org/obo/mondo#rare http://purl.obolibrary.org/obo/mondo#orphanet_rare http://purl.obolibrary.org/obo/mondo#gard_rare http://purl.obolibrary.org/obo/mondo#disease_grouping http://purl.obolibrary.org/obo/mondo#ordo_group_of_disorders |
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label |
congenital hypogonadotropic hypogonadism |
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notation |
MONDO:0015770 |
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prefLabel |
congenital hypogonadotropic hypogonadism |
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subClassOf |