Phenotypes for disease #00041 (PEOA3 (ophthalmoplegia, external, progressive, with mitochondrial DNA deletions, autosomal dominant, type 3 (PEOA-3)), OMIM:609286)

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AscendingPhenotype ID     

Diagnosis/Initial     

Inheritance     

Age/Examination     

Diagnosis/Definite     

Age/Diagnosis     

Age/Onset     

Phenotype/Onset     

Phenotype details     

Protein     

Owner     

Individual ID     
0000274655 - Familial - Mitochondrial DNA depletion syndrome type 7 - - - ID; muscle weakness; seizures; decreased mitochondrial respiratory chain complex activity (Neurological) - LOVD 00380802
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