PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS, AUTOSOMAL RECESSIVE 5; PEOB5

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:618098 - PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS, AUTOSOMAL RECESSIVE 5; PEOB5

Xenbase Genes: top3a

Human Disease Resource: OMIM

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0020845 - progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal recessive 5

MONDO:0020845 - progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal recessive 5

Disease Ontology (DO):

DOID:0111524 - autosomal recessive progressive external ophthalmoplegia with mitochondrial DNA deletions 5

DOID:0111524 - autosomal recessive progressive external ophthalmoplegia with mitochondrial DNA deletions 5