autosomaal dominante hereditaire aandoening
geïsoleerde agammaglobulinemie
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Autosomal dominant agammaglobulinemia due to E47 transcription factor deficiency (disorder)
Autosomal dominant agammaglobulinemia due to E47 transcription factor deficiency
Autosomal dominant agammaglobulinemia due to TCF3 mutation
Id1351668001
StatusPrimitive
Occurrencecongenitaal
Pathological processafwijkend immuunproces
SNOMED CT to ICD-10 extended map
TargetD80.0
RuleTRUE
AdviceALWAYS D80.0 | POSSIBLE REQUIREMENT FOR ADDITIONAL CODE TO FULLY DESCRIBE DISEASE OR CONDITION
CorrelationSNOMED CT source code to target map code correlation not specified