autosomaal dominante ernstige congenitale neutropenie
|
Autosomal dominant severe congenital neutropenia due to growth factor independent 1 transcriptional repressor gene mutation (disorder)
Autosomal dominant severe congenital neutropenia due to GFI1 mutation
Autosomal dominant severe congenital neutropenia due to growth factor independent 1 transcriptional repressor gene mutation
Id1386284002
StatusPrimitive
Occurrencecongenitaal
Pathological processafwijkend immuunproces
Has interpretationonder referentiebereik
Interpretsbepalen van neutrofielen
SNOMED CT to ICD-10 extended map
TargetD70
RuleTRUE
AdviceALWAYS D70 | POSSIBLE REQUIREMENT FOR ADDITIONAL CODE TO FULLY DESCRIBE DISEASE OR CONDITION
CorrelationSNOMED CT source code to target map code correlation not specified