X-linked immune dysregulation, polyendocrinopathy, enteropathy syndrome 724276006
SNOMED CT code
SNOMED code | 724276006 |
---|---|
name | X-linked immune dysregulation, polyendocrinopathy, enteropathy syndrome |
status | active |
date introduced | 2017-07-31 |
fully specified name(s) | X-linked immune dysregulation, polyendocrinopathy, enteropathy syndrome (disorder) |
synonyms |
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attributes - group3 | |
Associated with | Chromosomal disorder 409709004 |
attributes - group4 | |
Occurrence | Congenital 255399007 |
Finding site | Endocrine structure 113331007 |
Pathological process | Autoimmune process 263680009 |
attributes - group5 | |
Occurrence | Congenital 255399007 |
Finding site | Small intestinal structure 30315005 |
Pathological process | Autoimmune process 263680009 |
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 Sex-linked hereditary disorder 82852009 X-linked hereditary disease 128430005 X-linked recessive hereditary disease 1162976004 X-linked immune dysregulation, polyendocrinopathy, enteropathy syndrome 724276006 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Disorder of immune function 414029004 Immunodeficiency disorder 234532001 Primary immune deficiency disorder 58606001 Immunodeficiency associated with chromosomal abnormality 234632005 X-linked immune dysregulation, polyendocrinopathy, enteropathy syndrome 724276006 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Disorder of immune function 414029004 Autoimmune disease 85828009 Autoimmune enteropathy 235728001 X-linked immune dysregulation, polyendocrinopathy, enteropathy syndrome 724276006 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Disorder of body system 362965005 Disorder of endocrine system 362969004 Autoimmune endocrine disease 237822008 X-linked immune dysregulation, polyendocrinopathy, enteropathy syndrome 724276006 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Congenital disease 66091009 Congenital immunodeficiency disease 36138009 X-linked immune dysregulation, polyendocrinopathy, enteropathy syndrome 724276006 SNOMED CT Concept 138875005 Clinical finding 404684003 Digestive system finding 386617003 Disorder of digestive system 53619000 Digestive system hereditary disorder 363080007 X-linked immune dysregulation, polyendocrinopathy, enteropathy syndrome 724276006 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Disorder of body system 362965005 Disorder of endocrine system 362969004 Hereditary disorder of endocrine system 363104002 X-linked immune dysregulation, polyendocrinopathy, enteropathy syndrome 724276006 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Disorder of immune function 414029004 Hereditary disorder of immune system 363138005 X-linked immune dysregulation, polyendocrinopathy, enteropathy syndrome 724276006 |
ancestors | sorted most to least specific
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cpt crosswalks |
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