Huntington disease-like 2 721228006
SNOMED CT code
| SNOMED code | 721228006 |
|---|---|
| name | Huntington disease-like 2 |
| status | active |
| date introduced | 2017-01-31 |
| fully specified name(s) | Huntington disease-like 2 (disorder) |
| synonyms | Huntington disease-like 2 |
| attributes - group1 | |
| Associated morphology | Degenerative abnormality 107669003 |
| Finding site | Basal ganglion structure 32610002 |
| attributes - group3 | |
| Interprets | Movement 255324009 |
| attributes - group2 | |
| Interprets | Movement observable 363847004 |
| Has interpretation | Abnormal 263654008 |
| parents | |
| 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 Huntington disease-like 2 721228006 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Genetic disease 782964007 Hereditary disease 32895009 Autosomal hereditary disorder 1899006 Autosomal dominant hereditary disorder 11164009 Huntington disease-like 2 721228006 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Degenerative disorder 362975008 Degenerative disease of the central nervous system 80690008 Degenerative brain disorder 52522001 Cerebral degeneration 418143002 Huntington disease-like 2 721228006 SNOMED CT Concept 138875005 Clinical finding 404684003 Finding of movement 298325004 Involuntary movement 267078001 Chorea 271700006 Huntington disease-like syndrome 702376003 Huntington disease-like 2 721228006 |
| ancestors | sorted most to least specific
|
| cpt crosswalks | |
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