autosomaal recessieve hereditaire aandoening
congenitale agammaglobulinemie
hartziekte
hereditaire aandoening van cardiovasculair systeem
hereditaire aandoening van immuunsysteem
|||||
Autosomal recessive agammaglobulinemia due to folliculin interacting protein 1 deficiency (disorder)
Autosomal recessive agammaglobulinemia due to FNIP1 deficiency
Autosomal recessive agammaglobulinemia due to folliculin interacting protein 1 deficiency
Agammaglobulinemia due to FNIP1 defect
Id1351648007
StatusPrimitive
Occurrencecongenitaal
Pathological processafwijkend immuunproces
Finding sitestructuur van hart
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