Hyperimmunoglobulin M syndrome type 3 (disorder) | | Hyperimmunoglobulin M syndrome type 3 | | Hyper-IgM syndrome due to CD40 deficiency Autosomal recessive combined immunodeficiency due to CD40 mutation HIGM3 - hyperimmunoglobulin M syndrome type 3
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| Id | 1362020006 | 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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