autosomaal dominante hereditaire aandoening	common variable immunodeficiency	hereditaire aandoening van immuunsysteem
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Autosomal dominant combined variable immunodeficiency due to SEC61 translocon subunit alpha 1 mutation (disorder)
	Autosomal dominant combined variable immunodeficiency due to SEC61A1 mutation
	Autosomal dominant CVID (combined variable immunodeficiency) due to SEC61A1 deficiency Autosomal dominant combined variable immunodeficiency due to SEC61A1 deficiency Autosomal dominant combined variable immunodeficiency due to SEC61 translocon subunit alpha 1 mutation

Id	1354480001
Status	Primitive

Finding site	structuur van immuunsysteem
Pathological process	afwijkend immuunproces

SNOMED CT to ICD-10 extended map

Target	D83.8
Rule	TRUE
Advice	ALWAYS D83.8
Correlation	SNOMED CT source code to target map code correlation not specified