Rolandic epilepsy, speech dyspraxia syndrome 765093009
SNOMED CT code
| SNOMED code | 765093009 |
|---|---|
| name | Rolandic epilepsy, speech dyspraxia syndrome |
| status | active |
| date introduced | 2018-07-31 |
| fully specified name(s) | Rolandic epilepsy, speech dyspraxia syndrome (disorder) |
| synonyms | Rolandic epilepsy, speech dyspraxia syndrome |
| attributes - group2 | |
| Interprets | Ability to perform functions related to communication 288547000 |
| Has interpretation | Abnormal 263654008 |
| attributes - group3 | |
| Pathological process | Pathological developmental process 308490002 |
| attributes - group1 | |
| Occurrence | Congenital 255399007 |
| Finding site | Cerebrum 83678007 |
| parents | |
| hierarchies | a selection of possible paths SNOMED CT Concept 138875005Clinical finding 404684003 Functional finding 118228005 Communication disorder 278919001 Speech and language disorder 231543005 Speech and language dyspraxias 278920007 Rolandic epilepsy, speech dyspraxia syndrome 765093009 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Developmental disorder 5294002 Developmental hereditary disorder 363070008 Rolandic epilepsy, speech dyspraxia syndrome 765093009 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, speech dyspraxia syndrome 765093009 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Idiopathic disease 41969006 Localization-related idiopathic epilepsy 278510009 Benign Rolandic epilepsy 44145005 Rolandic epilepsy, speech dyspraxia syndrome 765093009 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Congenital disease 66091009 Rolandic epilepsy, speech dyspraxia syndrome 765093009 |
| ancestors | sorted most to least specific
|
| cpt crosswalks | |
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