Disease #04188 (ODG (dysgenesis, ovarian (ODG)))

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	ODG
Name	dysgenesis, ovarian (ODG)
OMIM ID	-
Inheritance	-
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 2 genes	ESR2, SOHLH1
Associated tissues	-
Disease features	-
Remarks	-
Date created	2015-02-14 15:50:42 +01:00 (CET)
Date last edited	2019-08-08 15:42:52 +02:00 (CEST)

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