Combined immunodeficiency due to OX40 deficiency 766879006
SNOMED CT code
| SNOMED code | 766879006 |
|---|---|
| name | Combined immunodeficiency due to OX40 deficiency |
| status | active |
| date introduced | 2018-07-31 |
| fully specified name(s) | Combined immunodeficiency due to OX40 deficiency (disorder) |
| synonyms |
|
| attributes - group3 | |
| Pathological process | Abnormal immune process 769247005 |
| attributes - group1 | |
| Finding site | Immune system structure 116003000 |
| Occurrence | Congenital 255399007 |
| attributes - group2 | |
| Due to | Chromosomal disorder 409709004 |
| parents |
|
| hierarchies | a selection of possible paths SNOMED CT Concept 138875005Clinical finding 404684003 Disease 64572001 Disorder of immune function 414029004 Immunodeficiency disorder 234532001 Primary immune deficiency disorder 58606001 Immunodeficiency associated with chromosomal abnormality 234632005 Combined immunodeficiency due to OX40 deficiency 766879006 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Congenital disease 66091009 Congenital immunodeficiency disease 36138009 Combined immunodeficiency due to OX40 deficiency 766879006 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Disorder of immune function 414029004 Hereditary disorder of immune system 363138005 Combined immunodeficiency due to OX40 deficiency 766879006 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Disorder of body system 362965005 Disorder of immune structure 414030009 Combined immunodeficiency due to OX40 deficiency 766879006 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Disorder of immune function 414029004 Immunodeficiency disorder 234532001 Primary immune deficiency disorder 58606001 Combined immunodeficiency disease 442459007 Combined immunodeficiency due to OX40 deficiency 766879006 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Genetic disease 782964007 Hereditary disease 32895009 Hereditary cancer-predisposing syndrome 699346009 Combined immunodeficiency due to OX40 deficiency 766879006 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Genetic disease 782964007 Hereditary disease 32895009 Autosomal hereditary disorder 1899006 Autosomal recessive hereditary disorder 85995004 Combined immunodeficiency due to OX40 deficiency 766879006 |
| ancestors | sorted most to least specific
|
| cpt crosswalks | |
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