Disease #07147 (HH26 (hypogonadotropic hypogonadism, type 26, with or without anosmia), OMIM:619718)

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Official abbreviation	HH26
Name	hypogonadotropic hypogonadism, type 26, with or without anosmia
OMIM ID	619718
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal dominant, Autosomal recessive
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	TCF12
Associated tissues	-
Disease features	-
Remarks	-
Date created	2025-01-23 09:25:40 +01:00 (CET)
Date last edited	N/A

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