congenitale neutropenie
hereditaire aandoening van leukocyt
trichothiodystrofie
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syndroom van onychotrichodysplasie en neutropenie (aandoening)
syndroom van onychotrichodysplasie en neutropenie
onychotrichodysplasie met neutropenie
trichothiodystrofie type G
Onycho-tricho-dysplasia neutropenia syndrome
Trichothiodystrophy type G
Id1003381002
StatusPrimitive
Associated morphologydysplasie
Finding sitestructuur van ectoderm
Occurrencecongenitaal
Pathological processproces van pathologische ontwikkeling
Associated morphologymorfologische afwijking
Finding sitestructuur van scapus
Occurrencecongenitaal
Pathological processproces van pathologische ontwikkeling
Has interpretationonder referentiebereik
Interpretsbepalen van neutrofielen
Pathological processafwijkend immuunproces
SNOMED CT to ICD-10 extended map
TargetL67.8
RuleTRUE
AdviceALWAYS L67.8 | POSSIBLE REQUIREMENT FOR ADDITIONAL CODE TO FULLY DESCRIBE DISEASE OR CONDITION
CorrelationSNOMED CT source code to target map code correlation not specified
TargetD70
RuleTRUE
AdviceALWAYS D70
CorrelationSNOMED CT source code to target map code correlation not specified