All diseases

OMIM ID
530000
OMIM term:
KEARNS-SAYRE SYNDROME; KSS
Alternative terms:
OPHTHALMOPLEGIA, PIGMENTARY DEGENERATION OF RETINA, AND CARDIOMYOPATHY
OCULOCRANIOSOMATIC SYNDROME
OPHTHALMOPLEGIA-PLUS SYNDROME
MITOCHONDRIAL CYTOPATHY
OPHTHALMOPLEGIA, PROGRESSIVE EXTERNAL, WITH RAGGED-RED FIBERS
CHRONIC PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MYOPATHY
CPEO WITH MYOPATHY
CPEO WITH RAGGED-RED FIBERS
(∗) Location:
(†) Associated OMIM genes:
(‡) Associated MGI genes:

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