autosomaal recessieve hereditaire aandoening
gecombineerde immunodeficiëntie
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Autosomal recessive combined immunodeficiency due to mannosidase alpha class 2B member 2 mutation (disorder)
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