autosomaal dominante hereditaire aandoening	hereditaire aandoening van bewegingsapparaat	hereditaire myopathie	hereditaire ontwikkelingsstoornis	myopathie met cytoplasmatische inclusielichaampjes
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hereditaire 'inclusion body'-myopathie type 4 (aandoening)
	hereditaire 'inclusion body'-myopathie type 4
	hereditaire IBM type 4 erfelijke inclusielichaammyopathie type 4
	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.

Id	770786001
Status	Primitive

Associated morphology	morfologische afwijking
Finding site	structuur van skeletspier
Occurrence	congenitaal
Pathological process	proces van pathologische ontwikkeling

DHD Diagnosis thesaurus reference set

RIVM authorized national diagnosis thesaurus to ICD10 complex mapping reference set

Target	G71.8
Term	Overige gespecificeerde primaire spieraandoeningen

SNOMED CT to Orphanet simple map

324381

SNOMED CT to ICD-10 extended map

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