Autosomal dominant hereditary disorder	Autosomal dominant 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
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Inclusion body myopathy with early-onset Paget disease and frontotemporal dementia (disorder)
	Inclusion body myopathy with early-onset Paget disease and frontotemporal dementia
	Muscular dystrophy limb-girdle with Paget disease of bone IBMPFD - Inclusion body myopathy with early onset Paget disease and frontotemporal dementia Pagetoid neuroskeletal syndrome Lower motor neuron degeneration with Paget-like bone disease Pagetoid amyotrophic lateral sclerosis
	'inclusion body'-myopathie met vroeg begin van ziekte van Paget en frontotemporale dementie
	IBMPFD

Id	703544004
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