Disease #05856 (ODG5 (dysgenesis, ovarian, type 5 (ODG5)), OMIM:617690)

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Official abbreviation	ODG5
Name	dysgenesis, ovarian, type 5 (ODG5)
OMIM ID	617690
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal recessive
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	SOHLH1
Associated tissues	-
Disease features	-
Remarks	-
Date created	2020-10-19 11:11:29 +02:00 (CEST)
Date last edited	N/A

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