Disease #03745 (HH11 (hypogonadism, hypogonadotropic, type 11 with/without anosmia (HH-11)), OMIM:614840)

Official abbreviation HH11
Name hypogonadism, hypogonadotropic, type 11 with/without anosmia (HH-11)
OMIM ID 614840
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease -
Phenotype entries for this disease -
Associated with 1 gene TACR3
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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