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ONTOLOGY REPORT - ANNOTATIONS


Term:Progressive External Ophthalmoplegia with Mitochondrial DNA Deletions, Autosomal Recessive 2
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Accession:DOID:9007961 term browser browse the term
Status:
This term is obsolete. We suggest searching for the text of the ontology term or for a keyword rather than searching for the ontology ID. For more information, please contact us.
Definition:A mitochondrial disorder characterized by adult onset of progressive external ophthalmoplegia, exercise intolerance, muscle weakness, and signs and symptoms of spinocerebellar ataxia, such as impaired gait and dysarthria. (OMIM)
Synonyms:exact_synonym: PEOB2;   PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA, AUTOSOMAL RECESSIVE 2
 replaced_by: DOID:0111515
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