PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS, AUTOSOMAL RECESSIVE 2; PEOB2

Click here to close Hello! We notice that you are using Internet Explorer, which is not supported by Xenbase and may cause the site to display incorrectly. We suggest using a current version of Chrome, FireFox, or Safari.

Summary

Literature (0)

MIM:616479 - PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS, AUTOSOMAL RECESSIVE 2; PEOB2

Xenbase Genes: rnaseh1

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0014656 - progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal recessive 2
MONDO:0018002 - adult-onset chronic progressive external ophthalmoplegia with mitochondrial myopathy

MONDO:0014656 - progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal recessive 2

MONDO:0018002 - adult-onset chronic progressive external ophthalmoplegia with mitochondrial myopathy

Disease Ontology (DO):

DOID:0111515 - autosomal recessive progressive external ophthalmoplegia with mitochondrial DNA deletions 2

DOID:0111515 - autosomal recessive progressive external ophthalmoplegia with mitochondrial DNA deletions 2