GenTIGSA Gene Database on Rare Genetic Disorders
Kearns-Sayre Syndrome  
Disease Aliases (10)

Chronic progressive external ophthalmoplegia with myopathy

Chronic progressive external ophthalmoplegia with myopathy, somatic

Cpeo with myopathy

Cpeo with ragged red fibers

Kearns-sayre mitochondrial cytopathy

Kss - kearns-sayre syndrome

Mitochondrial ocular myopathy

Oculocraniosomatic syndrome

Ophthalmoplegia plus syndrome

Ophthalmoplegia, pigmentary degeneration of retina, and cardiomyopathy

Associated Genes (0)
 

Cross-references of Kearns-Sayre syndrome OMIM GARD Orphanet NCBI-GTR NCBI-MedGen MalaCards      MeSH Annotations