Global Variome shared LOVD

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Phenotype #0000361378 Individual ID 00476704 Associated disease mitochondrial Diagnosis/Initial mitochondrial disease Diagnosis/Definite MTDPS13 Phenotype details see paper; ..., cardiomyopathy; gastrointestinal anomalies; elevated lactic level acid; normal creatine kinase level; no ragged red fibers; mitochondrial myopathy; cranial MRI encephalopathic lesions involving white matter, deep gray nuclei, and brainstem Inheritance Familial, autosomal recessive Age/Examination 8y (8 years) Age/Diagnosis - Age/Onset 1y Phenotype/Onset - Owner name Johan den Dunnen Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International 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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