Phenotype #0000361381

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Individual ID	00476707
Associated disease	mitochondrial
Diagnosis/Initial	mitochondrial disease
Diagnosis/Definite	-
Phenotype details	see paper; ..., no cardiomyopathy; no gastrointestinal anomalies; elevated lactic level acid; normal creatine kinase level; mild myopathy; cranial MRI T2-weighted hyperintensities in basal ganglia
Inheritance	Maternal, mitochondrial
Age/Examination	13y (13 years)
Age/Diagnosis	-
Age/Onset	4y
Phenotype/Onset	-
Owner name	Johan den Dunnen
Database submission license
Created by	Johan den Dunnen
Date created	2026-04-16 19:04:47 +02:00 (CEST)
Date last edited	N/A

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