Cockayne syndrome 21086008
SNOMED CT code
| SNOMED code | 21086008 |
|---|---|
| name | Cockayne syndrome |
| status | active |
| date introduced | 2002-01-31 |
| fully specified name(s) | Cockayne syndrome (disorder) |
| synonyms | Cockayne syndrome |
| attributes - group1 | |
| Pathological process | Pathological developmental process 308490002 |
| Associated morphology | Morphologically abnormal structure 49755003 |
| Occurrence | Congenital 255399007 |
| Finding site | Central nervous system structure 21483005 |
| parents | |
| children | |
| hierarchies | a selection of possible paths SNOMED CT Concept 138875005Clinical finding 404684003 Disease 64572001 Developmental disorder 5294002 Congenital malformation 276654001 Congenital malformation syndrome 400038003 Multiple system malformation syndrome 82354003 Multiple malformation syndrome with senile-like appearance 12674005 Cockayne syndrome 21086008 SNOMED CT Concept 138875005 Clinical finding 404684003 Central nervous system finding 246556002 Disorder of the central nervous system 23853001 Congenital anomaly of central nervous system 128124001 Cockayne syndrome 21086008 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Developmental disorder 5294002 Developmental hereditary disorder 363070008 Cockayne syndrome 21086008 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Disorder of body system 362965005 Disorder of nervous system 118940003 Hereditary disorder of nervous system 363235000 Cockayne syndrome 21086008 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Genetic disease 782964007 Hereditary disease 32895009 Hereditary cancer-predisposing syndrome 699346009 Cockayne syndrome 21086008 |
| ancestors | sorted most to least specific
|
| cpt crosswalks | |
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