| Autosomal recessive combined immunodeficiency due to complete interleukin 6 cytokine family signal transducer deficiency (disorder) | | Autosomal recessive combined immunodeficiency due to complete IL6ST deficiency | | Autosomal recessive combined immunodeficiency due to complete interleukin 6 cytokine family signal transducer deficiency
Stüve Wiedemann syndrome type 2
Autosomal recessive combined immunodeficiency due to complete IL6 signal transducer protein deficiency
Autosomal recessive hyperimmunoglobulin E syndrome due to complete IL6ST deficiency
Autosomal recessive combined immunodeficiency due to complete glycoprotein 130 deficiency
Autosomal recessive combined immunodeficiency due to GP130 deficiency
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| | Id | 1351328007 | | Status | Primitive |
| SNOMED CT to ICD-10 extended map | | Target | D82.4 | | Rule | TRUE | | Advice | ALWAYS D82.4 | 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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