Disease #03870 (HH17 (hypogonadism, hypogonadotropic, type 17 with/without anosmia (HH-17)), OMIM:615266)

Official abbreviation	HH17
Name	hypogonadism, hypogonadotropic, type 17 with/without anosmia (HH-17)
OMIM ID	615266
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal dominant
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	SPRY4
Associated tissues	-
Disease features	-
Remarks	-
Date created	2014-09-25 23:29:40 +02:00 (CEST)
Date last edited	2021-12-10 21:51:32 +01:00 (CET)

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Global Variome shared LOVD