Disease #06978 (OPDM4 (myopathy, oculopharyngodistal, type 4), OMIM:619790)

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Official abbreviation	OPDM4
Name	myopathy, oculopharyngodistal, type 4
OMIM ID	619790
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal dominant
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	RILPL1
Associated tissues	-
Disease features	-
Remarks	-
Date created	2022-11-27 16:03:51 +01:00 (CET)
Date last edited	N/A

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