Disease #03783 (HH16 (hypogonadism, hypogonadotropic, type 16 with/without anosmia (HH-16)), OMIM:614897)

Official abbreviation HH16
Name hypogonadism, hypogonadotropic, type 16 with/without anosmia (HH-16)
OMIM ID 614897
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease -
Phenotype entries for this disease -
Associated with 1 gene SEMA3A
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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