Disease #07136 (POF23 (ovarian failure, premature, type 23), OMIM:620686)

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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	Curator: Global Variome, with Curator vacancy

Official abbreviation	POF23
Name	ovarian failure, premature, type 23
OMIM ID	620686
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal recessive
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	MEIOB
Associated tissues	-
Disease features	-
Remarks	-
Date created	2024-11-24 14:34:46 +01:00 (CET)
Date last edited	N/A

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