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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
Id1351946008
StatusPrimitive
Pathological processafwijkend immuunproces
SNOMED CT to ICD-10 extended map
TargetD81.8
RuleTRUE
AdviceALWAYS D81.8 | POSSIBLE REQUIREMENT FOR ADDITIONAL CODE TO FULLY DESCRIBE DISEASE OR CONDITION
CorrelationSNOMED CT source code to target map code correlation not specified