Phenotypes for disease #01695 (Sengers;MTDPS10 (Senger syndrome (mitochondrial DNA depletion syndrome, type 10 (cardiomyopathic type, MTDPS-10))), OMIM:212350)

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AscendingPhenotype ID     

Phenotype details     

Diagnosis/Initial     

Diagnosis/Definite     

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Age/Diagnosis     

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Owner     

Individual ID     
0000301669 best corrected visual acuity: 0.5; electroretinogram , rod: n.a., cone: n.a. - dystrophy, corneoretinal, crystalline, Bietti (BCD) Familial, autosomal recessive 51y 36y - - - LOVD 00409552
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