autosomaal dominante hereditaire aandoening	hyper-IgE-syndroom
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autosomaal dominant hyperimmunoglobuline E-syndroom door deficiëntie van signaaltransductor en signaalactivator van transcriptie 3-proteïne (aandoening)
	autosomaal dominant hyperimmunoglobuline E-syndroom door deficiëntie van signaaltransductor en signaalactivator van transcriptie 3-proteïne
	syndroom van Job syndroom van Burkely AD-HIES door STAT3-deficiëntie autosomaal dominant hyper-IgE-syndroom door STAT3-deficiëntie
	Autosomal dominant hyper-IgE syndrome due to STAT3 deficiency
	Autosomal dominant hyperimmunoglobulin E syndrome due to signal transducer and activator of transcription 3 protein deficiency Job syndrome Buckley syndrome
	A very rare primary immunodeficiency disorder characterized by the clinical triad of high serum IgE (>2000 IU/ml), recurring staphylococcal skin abscesses, and recurrent pneumonia with formation of pneumatoceles.

Id	1351326006
Status	Primitive

Pathological process

afwijkend immuunproces

Has interpretation	boven referentiebereik
Interprets	bepalen van immunoglobuline E

SNOMED CT to ICD-10 extended map

Target	D82.4
Rule	TRUE
Advice	ALWAYS D82.4 \| POSSIBLE REQUIREMENT FOR ADDITIONAL CODE TO FULLY DESCRIBE DISEASE OR CONDITION
Correlation	SNOMED CT source code to target map code correlation not specified