Disease #06896 (OPDM3 (myopathy, oculopharyngodistal, type 3 (OPDM3)), OMIM:619473)

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Official abbreviation	OPDM3
Name	myopathy, oculopharyngodistal, type 3 (OPDM3)
OMIM ID	619473
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal dominant
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	NOTCH2NLC
Associated tissues	-
Disease features	-
Remarks	-
Date created	2022-02-13 13:51:32 +01:00 (CET)
Date last edited	N/A

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