Autosomal recessive hereditary disorder	Autosomal recessive hereditary disorder	Developmental hereditary disorder	Hereditary disorder of musculoskeletal system	Hereditary disorder of musculoskeletal system	Hereditary myopathy	Myopathy with cytoplasmic inclusions	Myopathy with cytoplasmic inclusions
\|	\|	\|	\|	\|	\|	\|	\|

Inclusion body myopathy 2 (disorder)
	Inclusion body myopathy 2
	Quadricep sparing inclusion body myopathy Distal myopathy with rimmed vacuoles Hereditary inclusion body myopathy Nonaka myopathy Rimmed vacuole myopathy
	'inclusion body'-myopathie type 2
	Nonaka-spierdystrofie distale myopathie met 'rimmed vacuoles' GNE-myopathie erfelijke 'inclusion body'-myopathie type 2 myopathie van Nonaka hereditaire inclusielichaammyopathie type 2 HIBM2 DMRV

Id	702382000
Status	Primitive

Associated morphology	Morphologically abnormal structure
Finding site	Skeletal muscle structure
Finding site	Skeletal muscle structure
Occurrence	Congenital
Occurrence	Congenital
Pathological process	Pathological developmental process

DHD Diagnosis thesaurus reference set

ICD-10 complex map reference set

Target	G71.8
Rule	TRUE
Advice	ALWAYS G71.8
Correlation	SNOMED CT source code to target map code correlation not specified