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Autosomal recessive common variable immunodeficiency due to POU class 2 homeobox associating factor 1 mutation (disorder)
Autosomal recessive common variable immunodeficiency due to POU2AF1 mutation
Autosomal recessive common variable immunodeficiency due to BOB1 deficiency
Autosomal recessive common variable immunodeficiency due to POU class 2 homeobox associating factor 1 mutation
Id1354596000
StatusPrimitive
SNOMED CT to ICD-10 extended map
TargetD83.8
RuleTRUE
AdviceALWAYS D83.8
CorrelationSNOMED CT source code to target map code correlation not specified