Autosomal dominant hereditary disorder	Autosomal dominant hereditary disorder	Congenital disease	Congenital myopathy	Disorder of skeletal muscle	Disorder of skeletal muscle	Hereditary disorder of musculoskeletal system	Hereditary disorder of musculoskeletal system	Hereditary myopathy
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Cap myopathy (disorder)
	Cap myopathy
	Cap disease Congenital myopathy with caps
	'cap'-myopathie

Id	703532002
Status	Primitive

Finding site	Skeletal muscle structure
Finding site	Skeletal muscle structure
Occurrence	Congenital
Occurrence	Congenital

DHD Diagnosis thesaurus reference set

ICD-10 complex map reference set

Target	G71.2
Rule	TRUE
Advice	ALWAYS G71.2
Correlation	SNOMED CT source code to target map code correlation not specified