Autosomal recessive hyperimmunoglobulin M syndrome 403836001
SNOMED CT code
| SNOMED code | 403836001 |
|---|---|
| name | Autosomal recessive hyperimmunoglobulin M syndrome |
| status | active |
| date introduced | 2003-07-31 |
| fully specified name(s) | Autosomal recessive hyperimmunoglobulin M syndrome (disorder) |
| synonyms |
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| attributes - group2 | |
| Pathological process | Abnormal immune process 769247005 |
| attributes - group1 | |
| Occurrence | Congenital 255399007 |
| parents | |
| hierarchies | a selection of possible paths SNOMED CT Concept 138875005Clinical finding 404684003 Disease 64572001 Congenital disease 66091009 Congenital immunodeficiency disease 36138009 Congenital hypergammaglobulinemia 58034007 Hyperimmunoglobulin M syndrome 82286005 Autosomal recessive hyperimmunoglobulin M syndrome 403836001 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Genetic disease 782964007 Hereditary disease 32895009 Autosomal hereditary disorder 1899006 Autosomal recessive hereditary disorder 85995004 Autosomal recessive hyperimmunoglobulin M syndrome 403836001 |
| ancestors | sorted most to least specific
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| cpt crosswalks | |
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