X-linked hyper-IgM syndrome 403835002
SNOMED CT code
| SNOMED code | 403835002 |
|---|---|
| name | X-linked hyper-IgM syndrome |
| status | active |
| date introduced | 2003-07-31 |
| fully specified name(s) | X-linked hyper-immunoglobulin M syndrome (disorder) |
| synonyms |
|
| 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 Genetic disease 782964007 Hereditary disease 32895009 Sex-linked hereditary disorder 82852009 X-linked hereditary disease 128430005 X-linked recessive hereditary disease 1162976004 X-linked hyper-IgM syndrome 403835002 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Congenital disease 66091009 Congenital immunodeficiency disease 36138009 Congenital hypergammaglobulinemia 58034007 Hyperimmunoglobulin M syndrome 82286005 X-linked hyper-IgM syndrome 403835002 |
| ancestors | sorted most to least specific
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| cpt crosswalks | |
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