Rolandic epilepsy, paroxysmal exercise-induced dystonia, writer's cramp syndrome 1231737000
SNOMED CT code
SNOMED code | 1231737000 |
---|---|
name | Rolandic epilepsy, paroxysmal exercise-induced dystonia, writer's cramp syndrome |
status | active |
date introduced | 2022-07-31 |
fully specified name(s) | Rolandic epilepsy, paroxysmal exercise-induced dystonia, writer's cramp syndrome (disorder) |
synonyms | Rolandic epilepsy, paroxysmal exercise-induced dystonia, writer's cramp syndrome |
attributes - group3 | |
Interprets | Movement 255324009 |
attributes - group1 | |
Finding site | Extrapyramidal system structure 76375004 |
attributes - group2 | |
Finding site | Cerebrum 83678007 |
attributes - group4 | |
Clinical course | Paroxysmal 26593000 |
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 Paroxysmal dystonia 230310003 Rolandic epilepsy, paroxysmal exercise-induced dystonia, writer's cramp syndrome 1231737000 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 Rolandic epilepsy, paroxysmal exercise-induced dystonia, writer's cramp syndrome 1231737000 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Idiopathic disease 41969006 Localization-related idiopathic epilepsy 278510009 Benign Rolandic epilepsy 44145005 Rolandic epilepsy, paroxysmal exercise-induced dystonia, writer's cramp syndrome 1231737000 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Genetic disease 782964007 Hereditary disease 32895009 Autosomal hereditary disorder 1899006 Autosomal recessive hereditary disorder 85995004 Rolandic epilepsy, paroxysmal exercise-induced dystonia, writer's cramp syndrome 1231737000 |
ancestors | sorted most to least specific
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cpt crosswalks |
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