Disease #06075 (POF11 (ovarian failure, premature, type 11), OMIM:616946)

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	POF11
Name	ovarian failure, premature, type 11
OMIM ID	616946
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal dominant
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	ERCC6
Associated tissues	-
Disease features	-
Remarks	-
Date created	2021-12-10 23:20:41 +01:00 (CET)
Date last edited	2022-02-16 19:58:03 +01:00 (CET)

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