Disease #05186 (POF17 (ovarian failure, premature, type 17), OMIM:619146)

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Official abbreviation	POF17
Name	ovarian failure, premature, type 17
OMIM ID	619146
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal recessive
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	XRCC2
Associated tissues	-
Disease features	-
Remarks	-
Date created	2016-10-04 15:15:43 +02:00 (CEST)
Date last edited	2022-04-07 19:00:58 +02:00 (CEST)

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