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.
DHD Diagnosis thesaurus reference set
RIVM authorized national diagnosis thesaurus to ICD10 complex mapping reference set
TermOverige gespecificeerde primaire spieraandoeningen
SNOMED CT to Orphanet simple map324381
SNOMED CT to ICD-10 extended map
AdviceALWAYS G71.8
CorrelationSNOMED CT source code to target map code correlation not specified