Benign adult familial myoclonic epilepsy 717225001
SNOMED CT code
| SNOMED code | 717225001 |
|---|---|
| name | Benign adult familial myoclonic epilepsy |
| status | active |
| date introduced | 2016-07-31 |
| fully specified name(s) | Benign adult familial myoclonic epilepsy (disorder) |
| synonyms |
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| attributes - group2 | |
| Finding site | Brain structure 12738006 |
| attributes - group1 | |
| Occurrence | Adulthood 41847000 |
| 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 Benign adult familial myoclonic epilepsy 717225001 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 Benign adult familial myoclonic epilepsy 717225001 SNOMED CT Concept 138875005 Clinical finding 404684003 Central nervous system finding 246556002 Finding of brain 299718000 Seizure 91175000 Seizure disorder 128613002 Epilepsy 84757009 Benign adult familial myoclonic epilepsy 717225001 |
| ancestors | sorted most to least specific
|
| cpt crosswalks | |
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