Prader-Willi-achtig syndroom
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SIM bHLH transcriptiefactor-1-gerelateerd Prader-Willi-achtig syndroom (aandoening)
SIM bHLH transcriptiefactor-1-gerelateerd Prader-Willi-achtig syndroom
SIM1-gerelateerd PWLS
SIM1-related Prader-Willi-like syndrome
SIM bHLH transcription factor 1-related Prader-Willi-like syndrome
Id1229943004
StatusPrimitive
Has interpretationboven referentiebereik
Interpretsmeetbare observatie betreffende lichaamsgewicht
Associated morphologymorfologische afwijking
Finding sitestructuur van aangezicht
Occurrencecongenitaal
Pathological processproces van pathologische ontwikkeling
Finding siteendocriene structuur van gonade
Occurrencecongenitaal
Pathological processproces van pathologische ontwikkeling
Finding sitestructuur van pars distalis adenohypophysis
Occurrencecongenitaal
Pathological processproces van pathologische ontwikkeling
SNOMED CT to Orphanet simple map398079
SNOMED CT to ICD-10 extended map
TargetQ87.1
RuleTRUE
AdviceALWAYS Q87.1 | POSSIBLE REQUIREMENT FOR ADDITIONAL CODE TO FULLY DESCRIBE DISEASE OR CONDITION
CorrelationSNOMED CT source code to target map code correlation not specified