Infantile-onset mesial temporal lobe epilepsy with severe cognitive regression 773421009
SNOMED CT code
| SNOMED code | 773421009 |
|---|---|
| name | Infantile-onset mesial temporal lobe epilepsy with severe cognitive regression |
| status | active |
| date introduced | 2019-01-31 |
| fully specified name(s) | Infantile-onset mesial temporal lobe epilepsy with severe cognitive regression (disorder) |
| synonyms | Infantile-onset mesial temporal lobe epilepsy with severe cognitive regression |
| attributes - group1 | |
| Occurrence | Infancy 3658006 |
| Finding site | Temporal lobe structure 78277001 |
| parents | |
| hierarchies | a selection of possible paths SNOMED CT Concept 138875005Clinical finding 404684003 Finding of head and neck region 118254002 Head finding 406122000 Finding of head region 298364001 Temporal lobe epilepsy 193000002 Infantile-onset mesial temporal lobe epilepsy with severe cognitive regression 773421009 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 Infantile-onset mesial temporal lobe epilepsy with severe cognitive regression 773421009 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Genetic disease 782964007 Hereditary disease 32895009 Autosomal hereditary disorder 1899006 Autosomal recessive hereditary disorder 85995004 Infantile-onset mesial temporal lobe epilepsy with severe cognitive regression 773421009 |
| ancestors | sorted most to least specific
|
| cpt crosswalks | |
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