PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS, AUTOSOMAL RECESSIVE 3; PEOB3

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Summary

Literature (0)

MIM:617069 - PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS, AUTOSOMAL RECESSIVE 3; PEOB3

Xenbase Genes: tk2

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0014898 - progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal recessive 3
MONDO:0016810 - autosomal recessive progressive external ophthalmoplegia

MONDO:0014898 - progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal recessive 3

MONDO:0016810 - autosomal recessive progressive external ophthalmoplegia