Disease #05643 (ODG8 (dysgenesis, ovarian, type 8 (ODG-8)), OMIM:618187)

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Official abbreviation	ODG8
Name	dysgenesis, ovarian, type 8 (ODG-8)
OMIM ID	618187
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal dominant
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	ESR2
Associated tissues	-
Disease features	-
Remarks	autosomal dominant
Date created	2019-08-08 15:44:06 +02:00 (CEST)
Date last edited	2021-12-10 21:51:32 +01:00 (CET)

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