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syndroom met calcinose, fenomeen van Raynaud, dysmotiliteit van oesofagus, sclerodactylie en teleangiëctasieën (aandoening)
CREST-syndroom
syndroom met calcinose, fenomeen van Raynaud, dysmotiliteit van oesofagus, sclerodactylie en teleangiëctasieën
CREST
gelimiteerde systemische sclerose
CREST-syndroom
Combinatie van verschijnselen: calcinose (kalkafzetting), Raynaud-fenomeen (verminderde bloedtoevoer), oesofagusdysmotiliteit (slokdarmklachten), sclerodactylie (verharde vingers), teleangiëctasieën (verwijde huidvaatjes).
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 morphologydystrofische calcificatie
Finding sitestructuur van huid
Associated morphologyteleangiëctasie
Associated morphologyfibrose
Finding sitestructuur van bindweefsel
Pathological processauto-immuunproces
General Practice / Family Practice reference set
DHD Diagnosis thesaurus reference set
RIVM authorized national diagnosis thesaurus to ICD10 complex mapping reference set
TargetM34.1
TermCR(E)ST syndrome
ICD-10 complex map reference set
TargetM34.1
RuleTRUE
AdviceALWAYS M34.1
CorrelationSNOMED CT source code to target map code correlation not specified