autosomaal dominante hereditaire aandoening	hyperimmunoglobuline M-syndroom zonder gevoeligheid voor opportunistische infectie
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Autosomal dominant hyperimmunoglobulin M syndrome due to activation induced cytidine deaminase deficiency (disorder)
	Autosomal dominant hyperimmunoglobulin M syndrome due to AID deficiency
	Autosomal dominant hyperimmunoglobulin M syndrome due to activation induced cytidine deaminase deficiency Autosomal dominant activation-induced cytidine deaminase deficiency Autosomal dominant hyper-IgM syndrome type 2 Autosomal dominant hyper IgM syndrome due to AICDA

Id	1351570003
Status	Primitive

Pathological process

afwijkend immuunproces

SNOMED CT to ICD-10 extended map

Target	D80.5
Rule	TRUE
Advice	ALWAYS D80.5 \| POSSIBLE REQUIREMENT FOR ADDITIONAL CODE TO FULLY DESCRIBE DISEASE OR CONDITION
Correlation	SNOMED CT source code to target map code correlation not specified