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Ontology Browser

Term:
Progressive External Ophthalmoplegia with Mitochondrial DNA Deletions, Autosomal Recessive 2 (DOID:9007961)
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Parent Terms Term With Siblings Child Terms
Progressive External Ophthalmoplegia with Mitochondrial DNA Deletions, Autosomal Recessive 2 
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 Synonyms: PEOB2 ;   PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA, AUTOSOMAL RECESSIVE 2
Replaced By: DOID:0111515

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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.