gecombineerde immunodeficiëntie
genetische aandoening
verhoogd immunoglobuline
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Hyperimmunoglobulin E syndrome (disorder)
Hyperimmunoglobulin E syndrome
HIES - hyperimmunoglobulin E syndrome
Hyper-IgE syndrome
Id191009009
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
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autosomaal recessief hyperimmunoglobuline E-syndroom door deficiëntie van zinkvingereiwit 341
Autosomal dominant combined immunodeficiency due to ERBIN deficiency
Autosomal dominant combined immunodeficiency due to partial IL6ST deficiency
Autosomal dominant hyper-IgE syndrome due to STAT3 deficiency
Autosomal recessive combined immunodeficiency due to complete IL6ST deficiency
Autosomal recessive combined immunodeficiency due to IL6R deficiency
Autosomal recessive combined immunodeficiency due to partial IL6ST deficiency
CADINS-ziekte
fosfoglucomutase-3-gerelateerd congenitaal defect in glycosylering
Netherton-syndroom