autosomaal dominante hereditaire aandoening
Hyperimmunoglobulin E syndrome
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Autosomal dominant combined immunodeficiency due to erbb2 interacting protein deficiency (disorder)
Autosomal dominant combined immunodeficiency due to ERBIN deficiency
Autosomal dominant hyperimmunoglobulin E syndrome due to ERBIN deficiency
Autosomal dominant combined immunodeficiency due to erbb2 interacting protein deficiency
Autosomal dominant hyperimmunoglobulin E syndrome due to ERBB2IP defect
Id1351324009
StatusPrimitive
Pathological processafwijkend immuunproces
Has interpretationboven referentiebereik
Interpretsbepalen van immunoglobuline E
SNOMED CT to ICD-10 extended map
TargetD82.4
RuleTRUE
AdviceALWAYS D82.4 | POSSIBLE REQUIREMENT FOR ADDITIONAL CODE TO FULLY DESCRIBE DISEASE OR CONDITION
CorrelationSNOMED CT source code to target map code correlation not specified