Disease #05742 (OPDM1 (myopathy, oculopharyngodistal, type 1 (OPDM1)), OMIM:164310)

Global Variome shared LOVD

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Official abbreviation	OPDM1
Name	myopathy, oculopharyngodistal, type 1 (OPDM1)
OMIM ID	164310
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal dominant, Autosomal recessive
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	LRP12
Associated tissues	-
Disease features	-
Remarks	-
Date created	2020-05-14 18:51:01 +02:00 (CEST)
Date last edited	N/A

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