Wilson's disease 88518009
SNOMED CT code
| SNOMED code | 88518009 |
|---|---|
| name | Wilson's disease |
| status | active |
| date introduced | 2002-01-31 |
| fully specified name(s) | Wilson's disease (disorder) |
| synonyms |
|
| attributes - group2 | |
| Associated morphology | Degenerative abnormality 107669003 |
| Finding site | Brain structure 12738006 |
| attributes - group1 | |
| Associated morphology | Degenerative abnormality 107669003 |
| Finding site | Liver structure 10200004 |
| attributes - group3 | |
| Associated morphology | Degenerative abnormality 107669003 |
| Finding site | Body tissue structure 85756007 |
| attributes - group4 | |
| Has interpretation | Abnormal 263654008 |
| Interprets | Movement observable 363847004 |
| attributes - group5 | |
| Finding site | Basal ganglion structure 32610002 |
| attributes - group6 | |
| Interprets | Movement 255324009 |
| parents |
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| children | |
| hierarchies | a selection of possible paths SNOMED CT Concept 138875005Clinical finding 404684003 Disease 64572001 Degenerative disorder 362975008 Degenerative disease of the central nervous system 80690008 Hereditary degenerative disease of central nervous system 106018006 Wilson's disease 88518009 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Metabolic disease 75934005 Metabolic and genetic disorder affecting the liver 235903001 Wilson's disease 88518009 SNOMED CT Concept 138875005 Clinical finding 404684003 Finding of movement 298325004 Involuntary movement 267078001 Chorea 271700006 Wilson's disease 88518009 SNOMED CT Concept 138875005 Clinical finding 404684003 Digestive system finding 386617003 Disorder of digestive system 53619000 Digestive system hereditary disorder 363080007 Wilson's disease 88518009 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Degenerative disorder 362975008 Degenerative disease of the central nervous system 80690008 Degenerative brain disorder 52522001 Wilson's disease 88518009 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Metabolic disease 75934005 Disorder of mineral metabolism 45744005 Disorder of copper metabolism 79886009 Wilson's disease 88518009 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Genetic disease 782964007 Hereditary disease 32895009 Autosomal hereditary disorder 1899006 Autosomal recessive hereditary disorder 85995004 Wilson's disease 88518009 |
| ancestors | sorted most to least specific
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| cpt crosswalks | |
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