Disease #03180 (HH6 (hypogonadotropic hypogonadism, type 6 with/without anosmia (HH6)), OMIM:612702)

Global Variome shared LOVD

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Official abbreviation	HH6
Name	hypogonadotropic hypogonadism, type 6 with/without anosmia (HH6)
OMIM ID	612702
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal dominant
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	FGF8
Associated tissues	-
Disease features	-
Remarks	-
Date created	2014-09-25 23:29:40 +02:00 (CEST)
Date last edited	2021-10-05 19:09:49 +02:00 (CEST)

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