autosomaal dominante hereditaire aandoening	common variable immunodeficiency	hereditaire aandoening van immuunsysteem
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autosomaal dominante 'common variable immunodeficiency' door mutatie in 'SEC61 translocon subunit alpha 1' (aandoening)
	autosomaal dominante 'common variable immunodeficiency' door mutatie in SEC61A1
	autosomaal dominante 'common variable immunodeficiency' door mutatie in 'SEC61 translocon subunit alpha 1' autosomaal dominante CVID door SEC61A1-deficiëntie autosomaal dominante 'common variable'-immunodeficiëntie door SEC61A1-mutatie
	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