Phenotypes for disease #06359 (PEOB5 (?Progressive external ophthalmoplegia with Mi DNA deletions, autosomal recessive 5), OMIM:618098)

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0000357040 Metabolic myopathy Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal recessive 5 Adult-onset chronic progressive external ophthalmoplegia with mitochondrial myopathy, Ptosis, Bilateral sensorineural hearing impairment, easy fatigability, progressive external ophtalmoplegia, exercice intolerance, hearing impairment, bilteral ptosis, weakness of facial musculature Unknown - - - - Camille Verebi 00472231
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