autosomaal recessieve hereditaire aandoening	gecombineerde immunodeficiëntie
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autosomaal recessieve gecombineerde immunodeficiëntie door mutatie in 'mannosidase alpha class 2B member 2' (aandoening)
	autosomaal recessieve gecombineerde immunodeficiëntie door mutatie in MAN2B2
	autosomaal recessieve gecombineerde immunodeficiëntie door MAN2B2-deficiëntie autosomaal recessieve gecombineerde immunodeficiëntie door mutatie in 'mannosidase alpha class 2B member 2'
	Autosomal recessive combined immunodeficiency due to MAN2B2 mutation
	Autosomal recessive combined immunodeficiency due to mannosidase alpha class 2B member 2 mutation Autosomal recessive combined immunodeficiency due to MAN2B2 deficiency

Id	1351946008
Status	Primitive

Pathological process

afwijkend immuunproces

SNOMED CT to ICD-10 extended map

Target	D81.8
Rule	TRUE
Advice	ALWAYS D81.8 \| POSSIBLE REQUIREMENT FOR ADDITIONAL CODE TO FULLY DESCRIBE DISEASE OR CONDITION
Correlation	SNOMED CT source code to target map code correlation not specified