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At a Glance
Cataract and cardiomyopathy; Ataxia-oculomotor apraxia type 1; Autosomal dominant progressive external ophthalmoplegia with mitochondrial DNA deletions 1 more...
AGK (7q34); APTX (9p21.1); DGUOK (2p13.1); DNA2 (10q21.3); FBXL4 (6q16.1-16.2) more...
Conditions Help
Total conditions: 27
Condition/Phenotype Identifier
Methodology
Total methods: 0
Method Category Help
Test method Help
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* Instrument: Not provided
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Additional Information

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