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Autosomal recessive hyperimmunoglobulin M syndrome due to uracil DNA glycosylase deficiency (disorder)
Autosomal recessive hyperimmunoglobulin M syndrome due to UNG deficiency
Autosomal recessive hyperimmunoglobulin M syndrome due to uracil DNA glycosylase deficiency
Hyper-IgM syndrome due to UNG
Hyper-IgM syndrome type 5
Hyper-IgM syndrome due to uracil N-glycosylase
Id1351569004
StatusPrimitive
Pathological processafwijkend immuunproces
SNOMED CT to ICD-10 extended map
TargetD80.5
RuleTRUE
AdviceALWAYS D80.5 | POSSIBLE REQUIREMENT FOR ADDITIONAL CODE TO FULLY DESCRIBE DISEASE OR CONDITION
CorrelationSNOMED CT source code to target map code correlation not specified