Mendelian susceptibility to mycobacterial disease due to partial IRF8 deficiency 723385003
SNOMED CT code
SNOMED code | 723385003 |
---|---|
name | Mendelian susceptibility to mycobacterial disease due to partial IRF8 deficiency |
status | active |
date introduced | 2017-07-31 |
fully specified name(s) | Mendelian susceptibility to mycobacterial disease due to partial interferon regulatory factor 8 deficiency (disorder) |
synonyms |
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attributes - group2 | |
Pathological process | Abnormal immune process 769247005 |
parents |
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hierarchies | a selection of possible paths SNOMED CT Concept 138875005Clinical finding 404684003 Disease 64572001 Genetic disease 782964007 Hereditary disease 32895009 Autosomal hereditary disorder 1899006 Autosomal dominant hereditary disorder 11164009 Mendelian susceptibility to mycobacterial disease due to partial IRF8 deficiency 723385003 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Genetic disease 782964007 Hereditary disease 32895009 Mendelian susceptibility to mycobacterial disease 1172895006 Mendelian susceptibility to mycobacterial disease due to partial IRF8 deficiency 723385003 |
ancestors | sorted most to least specific
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cpt crosswalks |
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