Autosomal dominant hereditary disorder	Developmental hereditary disorder	Hereditary disorder of musculoskeletal system	Hereditary myopathy	Myopathy with cytoplasmic inclusions
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Hereditary inclusion body myopathy type 4 (disorder)
	Hereditary inclusion body myopathy type 4
	A rare non-dystrophic myopathy with characteristics of slowly progressive muscular weakness and atrophy initially involving proximal lower limbs and hip girdle and later on shoulder girdle, proximal upper limbs and axial muscles. Ambulation is usually preserved. Congophilic inclusions with cytoplasmic inclusions of 15-21 nm filaments on electron microscopy are revealed in muscle biopsy.
	hereditaire 'inclusion body'-myopathie type 4
	hereditaire IBM type 4 erfelijke inclusielichaammyopathie type 4

Id	770786001
Status	Primitive

Associated morphology	Morphologically abnormal structure
Finding site	Skeletal muscle structure
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