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

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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