Chronic metabolic disorder	Hereditary disorder of musculoskeletal system	Hereditary disorder of nervous system	Hereditary disorder of the visual system	Hereditary metabolic disease	Hereditary myopathy	Mitochondrial myopathy	Myopathy of extraocular muscles	Progressive external ophthalmoplegia
\|	\|	\|	\|	\|	\|	\|	\|	\|

Adult-onset chronic progressive external ophthalmoplegia with mitochondrial myopathy (disorder)
	Adult-onset chronic progressive external ophthalmoplegia with mitochondrial myopathy
	Adult-onset CPEO (chronic progressive external ophthalmoplegia) with mitochondrial myopathy
	A rare mitochondrial disease with characteristics of adult onset of progressive external ophthalmoplegia, exercise intolerance, muscle weakness, manifestations of spinocerebellar ataxia (e.g. impaired gait, dysarthria) and mild motor peripheral neuropathy. Respiratory insufficiency has been reported in some cases.
	chronische progressieve externe oftalmoplegie met mitochondriale myopathie beginnend op volwassen leeftijd
	CPEO met mitochondriële myopathie beginnend op volwassen leeftijd

Id	725464001
Status	Primitive

Finding site	Skeletal muscle structure
Occurrence	Adulthood

Finding site	Eye region structure
Occurrence	Adulthood

Finding site	Structure of nervous system
Occurrence	Adulthood

Clinical course

Finding site

Structure of extraocular muscle

DHD Diagnosis thesaurus reference set

ICD-10 complex map reference set

Target	G71.3
Rule	TRUE
Advice	ALWAYS G71.3 \| POSSIBLE REQUIREMENT FOR ADDITIONAL CODE TO FULLY DESCRIBE DISEASE OR CONDITION
Correlation	SNOMED CT source code to target map code correlation not specified

Target	H49.4
Rule	TRUE
Advice	ALWAYS H49.4
Correlation	SNOMED CT source code to target map code correlation not specified