hypogonadotropic hypogonadism 3 with or without anosmia
Go to external page http://purl.obolibrary.org/obo/MONDO_0009482
Any hypogonadotropic hypogonadism in which the cause of the disease is a mutation in the PROKR2 gene. [ MONDO:patterns/disease_series_by_gene ]
Synonyms: PROKR2 hypogonadotropic hypogonadism hypogonadotropic hypogonadism 3 with or without anosmia hypogonadotropic hypogonadism caused by mutation in PROKR2
Term information
- DOID:0090092 (MONDO:equivalentTo)
- OMIM:244200 (MONDO:equivalentTo)
- ICD10CM:E23.0 (MONDO:relatedTo)
- GARD:3073 (OMIM:244200)
- UMLS:C3550478 (OMIM:244200)
gard_rare, rare, nord_rare, clingen
https://omim.org/entry/244200
http://linkedlifedata.com/resource/umls/id/C3550478
http://purl.obolibrary.org/obo/DOID_0090092