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syndroom met calcinose, fenomeen van Raynaud, dysmotiliteit van oesofagus, sclerodactylie en teleangiëctasieën (aandoening)
CREST-syndroom
CREST
gelimiteerde systemische sclerose
syndroom met calcinose, fenomeen van Raynaud, dysmotiliteit van oesofagus, sclerodactylie en teleangiëctasieën
CREST syndrome
Calcinosis, Raynaud's phenomenon, esophageal dysmotility, sclerodactyly, and telangiectasia syndrome
CREST - Calcinosis, Raynaud's phenomenon, sclerodactyly, esophageal involvement, telangiectasia syndrome
Calcinosis cutis, Raynaud's, esophageal dysfunction, sclerodactyly AND telangiectasia
Calcinosis, Raynaud phenomenon, esophageal dysmotility, sclerodactyly, and telangiectasia (CREST) syndrome
Calcinosis, Raynaud's phenomenon, esophageal dysmotility, sclerodactyly, and telangiectasia (CREST) syndrome
CREST - Calcinosis, Raynaud's phenomenon, esophageal dysfunction, sclerodactyly, telangiectasia
Id31848007
StatusPrimitive
Associated morphologyfibrose
Finding sitestructuur van bindweefsel
Pathological processauto-immuunproces
Finding sitestructuur van hand
Associated morphologydystrofische calcificatie
Finding sitestructuur van huid
Associated morphologyteleangiëctasie
General Practice / Family Practice reference set
ICD-10 complex map reference set
TargetM34.1
RuleTRUE
AdviceALWAYS M34.1
CorrelationSNOMED CT source code to target map code correlation not specified
International Classification of Primary Care, Second edition complex map reference set
TargetA99
RuleTRUE
AdviceALWAYS A99
CorrelationSNOMED CT source code to target map code correlation not specified