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Autosomal recessive common variable immunodeficiency due to Rac family small GTPase 2 deficiency (disorder)
Autosomal recessive common variable immunodeficiency due to RAC2 deficiency
Autosomal recessive CVID (common variable immunodeficiency) due to RAC2 mutation
Autosomal recessive common variable immunodeficiency due to Rac family small GTPase 2 deficiency
Autosomal recessive common variable immunodeficiency due to RAC2 mutation
Id1356782005
StatusPrimitive
SNOMED CT to ICD-10 extended map
TargetD83.8
RuleTRUE
AdviceALWAYS D83.8 | POSSIBLE REQUIREMENT FOR ADDITIONAL CODE TO FULLY DESCRIBE DISEASE OR CONDITION
CorrelationSNOMED CT source code to target map code correlation not specified