Mendelian susceptibility to mycobacterial disease due to complete interferon gamma receptor 1 deficiency 718230004
SNOMED CT code
| SNOMED code | 718230004 |
|---|---|
| name | Mendelian susceptibility to mycobacterial disease due to complete interferon gamma receptor 1 deficiency |
| status | active |
| date introduced | 2016-07-31 |
| fully specified name(s) | Mendelian susceptibility to mycobacterial disease due to complete interferon gamma receptor 1 deficiency (disorder) |
| synonyms |
|
| attributes - group2 | |
| Pathological process | Abnormal immune process 769247005 |
| parents |
|
| hierarchies | a selection of possible paths SNOMED CT Concept 138875005Clinical finding 404684003 Disease 64572001 Genetic disease 782964007 Hereditary disease 32895009 Mendelian susceptibility to mycobacterial disease 1172895006 Mendelian susceptibility to mycobacterial disease due to complete interferon gamma receptor 1 deficiency 718230004 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Genetic disease 782964007 Hereditary disease 32895009 Autosomal hereditary disorder 1899006 Autosomal recessive hereditary disorder 85995004 Mendelian susceptibility to mycobacterial disease due to complete interferon gamma receptor 1 deficiency 718230004 |
| ancestors | sorted most to least specific
|
| cpt crosswalks | |
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