Phenotype #0000003237

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	00004540
Associated disease	MYOP
Phenotype details	mtDNA depletion myopathy
Diagnosis/Initial	-
Inheritance	Familial, autosomal recessive
Diagnosis/Definite	-
Age/Examination	-
Age/Diagnosis	-
Age/Onset	-
Phenotype/Onset	-
Protein	-
Owner name	Robert McFarland
Database submission license	No license selected
Created by	Robert McFarland
Date created	2014-01-31 00:19:05 +01:00 (CET)
Date last edited	2014-02-02 22:08:51 +01:00 (CET)

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