Progressive myoclonic epilepsy type 7 1208939001
SNOMED CT code
| SNOMED code | 1208939001 |
|---|---|
| name | Progressive myoclonic epilepsy type 7 |
| status | active |
| date introduced | 2022-03-31 |
| fully specified name(s) | Progressive myoclonic epilepsy type 7 (disorder) |
| synonyms |
|
| attributes - group1 | |
| Clinical course | Progressive 255314001 |
| attributes - group3 | |
| Interprets | Movement 255324009 |
| attributes - group2 | |
| Finding site | Brain structure 12738006 |
| 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 Progressive myoclonic epilepsy type 7 1208939001 SNOMED CT Concept 138875005 Clinical finding 404684003 Central nervous system finding 246556002 Finding of brain 299718000 Seizure 91175000 Seizure disorder 128613002 Epilepsy 84757009 Progressive myoclonic epilepsy 267581004 Progressive myoclonic epilepsy type 7 1208939001 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 Progressive myoclonic epilepsy type 7 1208939001 SNOMED CT Concept 138875005 Clinical finding 404684003 Finding of movement 298325004 Movement disorder 60342002 Progressive myoclonic epilepsy type 7 1208939001 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Chronic disease 27624003 Chronic nervous system disorder 128283000 Chronic brain syndrome 78689005 Progressive myoclonic epilepsy type 7 1208939001 |
| ancestors | sorted most to least specific
|
| cpt crosswalks | |
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