Dopamine transporter deficiency syndrome 722763000
SNOMED CT code
| SNOMED code | 722763000 |
|---|---|
| name | Dopamine transporter deficiency syndrome |
| status | active |
| date introduced | 2017-01-31 |
| fully specified name(s) | Infantile dystonia parkinsonism (disorder) |
| synonyms |
|
| attributes - group3 | |
| Interprets | Movement 255324009 |
| Has interpretation | Slow 255361000 |
| attributes - group1 | |
| Occurrence | Infancy 3658006 |
| Finding site | Basal ganglion structure 32610002 |
| parents | |
| hierarchies | a selection of possible paths SNOMED CT Concept 138875005Clinical finding 404684003 Finding of movement 298325004 Movement disorder 60342002 Extrapyramidal disease 76349003 Dystonia 15802004 Dopamine transporter deficiency syndrome 722763000 SNOMED CT Concept 138875005 Clinical finding 404684003 Finding of movement 298325004 Bradykinesia 399317006 Parkinsonism 32798002 Dopamine transporter deficiency syndrome 722763000 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 Dopamine transporter deficiency syndrome 722763000 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Genetic disease 782964007 Hereditary disease 32895009 Autosomal hereditary disorder 1899006 Autosomal recessive hereditary disorder 85995004 Dopamine transporter deficiency syndrome 722763000 |
| ancestors | sorted most to least specific
|
| cpt crosswalks | |
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