Disease #07135 (POF25 (ovarian failure, premature, type 25), OMIM:621002)

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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	Curators: Gerard Pals, Sonna Stolk, Raymond Dalgleish, and Dimitra Micha

Official abbreviation	POF25
Name	ovarian failure, premature, type 25
OMIM ID	621002
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal recessive
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	SPATA22
Associated tissues	-
Disease features	-
Remarks	-
Date created	2024-11-24 14:14:34 +01:00 (CET)
Date last edited	N/A

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