Disease #04470 (HH22 (hypogonadism, hypogonadotropic, type 22 with/without anosmia (HH-22)), OMIM:616030)

Official abbreviation HH22
Name hypogonadism, hypogonadotropic, type 22 with/without anosmia (HH-22)
OMIM ID 616030
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease -
Phenotype entries for this disease -
Associated with 1 gene FEZF1
Associated tissues -
Disease features -
Remarks -
Date created 2015-09-23 10:25:22 +02:00 (CEST)
Date last edited 2021-12-10 21:51:32 +01:00 (CET)

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