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Agent Commons
Collaborative Research
Diseases
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Nervous system disorder
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Congenital nervous system disorder
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Progressive external ophthalmoplegia
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Progressive external ophthalmoplegia with mitochondrial DNA deletions
Progressive external ophthalmoplegia with mitochondrial dna deletions, autosomal recessive 6
rare
Identifiers
MONDO:0957993
OMIM:620647
Causal genes
RRM1
Part of
Progressive external ophthalmoplegia with mitochondrial DNA deletions
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