Familial focal epilepsy with variable foci 764522009
SNOMED CT code
| SNOMED code | 764522009 |
|---|---|
| name | Familial focal epilepsy with variable foci |
| status | active |
| date introduced | 2018-07-31 |
| fully specified name(s) | Familial focal epilepsy with variable foci (disorder) |
| synonyms |
|
| attributes - group1 | |
| Occurrence | Congenital 255399007 |
| Finding site | Cerebrum 83678007 |
| parents | |
| hierarchies | a selection of possible paths SNOMED CT Concept 138875005Clinical finding 404684003 Disease 64572001 Genetic disease 782964007 Hereditary disease 32895009 Autosomal hereditary disorder 1899006 Autosomal dominant hereditary disorder 11164009 Familial focal epilepsy with variable foci 764522009 SNOMED CT Concept 138875005 Clinical finding 404684003 Central nervous system finding 246556002 Finding of brain 299718000 Seizure 91175000 Seizure disorder 128613002 Epilepsy 84757009 Localization-related epilepsy 230381009 Localization-related symptomatic epilepsy 230390002 Familial focal epilepsy with variable foci 764522009 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 Familial focal epilepsy with variable foci 764522009 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Congenital disease 66091009 Familial focal epilepsy with variable foci 764522009 |
| ancestors | sorted most to least specific
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| cpt crosswalks | |
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