Phenotype #0000361386

Individual ID 00476712
Associated disease mitochondrial
Diagnosis/Initial mitochondrial disease
Diagnosis/Definite LGMDR2
Phenotype details see paper; ..., cardiomyopathy; no gastrointestinal anomalies; normal lactic level acid; elevated creatine kinase level; no ragged red fibers; mitochondrial myopathy; cranial MRI normal
Inheritance Familial, autosomal recessive
Age/Examination 42y (42 years)
Age/Diagnosis -
Age/Onset 22y
Phenotype/Onset -
Owner name Johan den Dunnen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons 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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