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
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| Id | 1351569004 | Status | Primitive |
SNOMED CT to ICD-10 extended map | Target | D80.5 | Rule | TRUE | Advice | ALWAYS D80.5 | POSSIBLE REQUIREMENT FOR ADDITIONAL CODE TO FULLY DESCRIBE DISEASE OR CONDITION | Correlation | SNOMED CT source code to target map code correlation not specified |
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