Phenotype #0000228676

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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	Curator: Global Variome, with Curator vacancy

Individual ID	00301564
Associated disease	OPDM
Diagnosis/Initial	oculopharyngodistal myopathy
Diagnosis/Definite	OPDM1
Phenotype details	ptosis, extraocular and pharyngeal weakness
Inheritance	Familial, autosomal dominant
Age/Examination	-
Age/Diagnosis	-
Age/Onset	-
Phenotype/Onset	-
Owner name	Johan den Dunnen
Database submission license
Created by	Johan den Dunnen
Date created	2020-05-18 19:42:58 +02:00 (CEST)
Date last edited	N/A

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