MeSH Browser

MeSH Supplementary: Progressive External Ophthalmoplegia With Mitochondrial Dna Deletions, Autosomal Dominant, 5
Unique ID: C567768
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C567768
Entry Term(s): Peoa5; Progressive External Ophthalmoplegia, Autosomal Dominant, 5
Registry Number: 0
Heading Mapped to: *Ophthalmoplegia, Chronic Progressive External; *Mitochondrial Diseases
Frequency: 0
Note: aka PEOA5; mutations in RRM2B
Date of Entry: 2012/08/24

Progressive External Ophthalmoplegia With Mitochondrial Dna Deletions, Autosomal Dominant, 5 MeSH Supplementary Concept Data 2024