autosomaal dominante 'limb-girdle' spierdystrofie
|
autosomaal dominante 'limb-girdle'-spierdystrofie type 1F (aandoening)
autosomaal dominante 'limb-girdle'-spierdystrofie type 1F
autosomaal dominante 'limb-girdle muscular dystrophy' type 1F
autosomaal dominante gordeldystrofie type 1F
LGMD1F
Autosomal dominant limb girdle muscular dystrophy type 1F
A form of limb girdle muscular dystrophy with characteristics of muscle weakness affecting the pelvic girdle and especially the iliopsoas muscle. Respiratory impairment may be observed in advanced stages.
Id719989007
StatusPrimitive
Associated morphologydystrofie
Finding sitestructuur van skeletspier
Pathological processproces van pathologische ontwikkeling
Clinical courseprogressief
DHD Diagnosis thesaurus reference set
RIVM authorized national diagnosis thesaurus to ICD10 complex mapping reference set
TargetG71.0
TermSpierdystrofie
SNOMED CT to Orphanet simple map55595
SNOMED CT to ICD-10 extended map
TargetG71.0
RuleTRUE
AdviceALWAYS G71.0
CorrelationSNOMED CT source code to target map code correlation not specified