Familial cortical myoclonus 763770005
SNOMED CT code
| SNOMED code | 763770005 |
|---|---|
| name | Familial cortical myoclonus |
| status | active |
| date introduced | 2018-07-31 |
| fully specified name(s) | Familial myoclonus of cerebral cortex (disorder) |
| synonyms |
|
| attributes - group2 | |
| Interprets | Movement 255324009 |
| attributes - group1 | |
| Finding site | Cerebral cortex 40146001 |
| 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 cortical myoclonus 763770005 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Familial disease 111941005 Familial cortical myoclonus 763770005 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 cortical myoclonus 763770005 SNOMED CT Concept 138875005 Clinical finding 404684003 Finding of movement 298325004 Movement disorder 60342002 Myoclonic disorder 127324008 Cerebral cortex myoclonus 698835006 Familial cortical myoclonus 763770005 |
| ancestors | sorted most to least specific
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| cpt crosswalks | |
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