Disease #03747 (HH13 (hypogonadism, hypogonadotropic, type 13 with/without anosmia (HH-13)), OMIM:614842)

Official abbreviation	HH13
Name	hypogonadism, hypogonadotropic, type 13 with/without anosmia (HH-13)
OMIM ID	614842
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal recessive
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	KISS1
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)

Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.

Global Variome shared LOVD