Autosomal recessive combined variable immunodeficiency due to B cell-activating factor receptor mutation (disorder) | | Autosomal recessive combined variable immunodeficiency due to BAFF receptor deficiency | | Autosomal recessive CVID (combined variable immunodeficiency) due to TNFRSF13C mutation Autosomal recessive combined variable immunodeficiency due to B cell-activating factor receptor mutation Autosomal recessive combined variable immunodeficiency due to BAFF-R deficiency Autosomal recessive combined variable immunodeficiency due to BAFF-R mutation
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| Id | 1352023006 | Status | Primitive |
SNOMED CT to ICD-10 extended map | Target | D83.0 | Rule | TRUE | Advice | ALWAYS D83.0 | Correlation | SNOMED CT source code to target map code correlation not specified |
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