Disease #05831 (OPDM2 (myopathy, oculopharyngodistal, type 2 (OPDM2)), OMIM:618940)

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Official abbreviation	OPDM2
Name	myopathy, oculopharyngodistal, type 2 (OPDM2)
OMIM ID	618940
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal dominant
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	GIPC1
Associated tissues	-
Disease features	-
Remarks	-
Date created	2020-09-14 08:55:11 +02:00 (CEST)
Date last edited	N/A

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