Kirman syndrome 239038006
SNOMED CT code
| SNOMED code | 239038006 |
|---|---|
| name | Kirman syndrome |
| status | active |
| date introduced | 2002-01-31 |
| fully specified name(s) | Kirman syndrome (disorder) |
| synonyms | Kirman syndrome |
| attributes - group1 | |
| Occurrence | Congenital 255399007 |
| Pathological process | Pathological developmental process 308490002 |
| Finding site | Ectoderm structure 63206006 |
| Associated morphology | Dysplasia 25723000 |
| attributes - group2 | |
| Associated morphology | Morphologically abnormal structure 49755003 |
| Pathological process | Pathological developmental process 308490002 |
| Finding site | Skin structure 39937001 |
| Occurrence | Congenital 255399007 |
| parents | Ectodermal dysplasia 8654005 |
| hierarchies | a selection of possible paths SNOMED CT Concept 138875005Clinical finding 404684003 Disease 64572001 Disorder of embryonic structure 609521009 Congenital ectodermal defect 254154003 Ectodermal dysplasia 8654005 Kirman syndrome 239038006 |
| ancestors | sorted most to least specific
|
| cpt crosswalks | |
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