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Progressive External Ophthalmoplegia with Mitochondrial DNA Deletions, Autosomal Dominant, 1 MeSH Supplementary Concept Data 2022


MeSH Supplementary
Progressive External Ophthalmoplegia with Mitochondrial DNA Deletions, Autosomal Dominant, 1
Unique ID
C563575
RDF Unique Identifier
http://id.nlm.nih.gov/mesh/C563575
Entry Term(s)
Progressive External Ophthalmoplegia, Autosomal Dominant, 1
Registry Number
0
Heading Mapped to
*Ophthalmoplegia
*Mitochondrial Diseases
Frequency
0
Date of Entry
2012/11/05
Progressive External Ophthalmoplegia with Mitochondrial DNA Deletions, Autosomal Dominant, 1 Preferred
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