Phenotype #0000274655

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Individual ID	00380802
Associated disease	PEOA3
Inheritance	Familial
Diagnosis/Initial	-
Age/Examination	-
Diagnosis/Definite	Mitochondrial DNA depletion syndrome type 7
Age/Diagnosis	-
Age/Onset	-
Phenotype/Onset	-
Phenotype details	ID; muscle weakness; seizures; decreased mitochondrial respiratory chain complex activity (Neurological)
Protein	-
Owner name	LOVD
Database submission license
Created by	Anna Tracewska
Date created	2021-08-23 12:15:23 +02:00 (CEST)
Date last edited	N/A

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