Benign familial neonatal-infantile seizures 1231282002
SNOMED CT code
| SNOMED code | 1231282002 |
|---|---|
| name | Benign familial neonatal-infantile seizures |
| status | active |
| date introduced | 2022-06-30 |
| fully specified name(s) | Benign familial neonatal-infantile seizures (disorder) |
| synonyms |
|
| attributes - group1 | |
| Occurrence | Infancy 3658006 |
| 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 Benign familial neonatal-infantile seizures 1231282002 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 familial neonatal-infantile seizures 1231282002 SNOMED CT Concept 138875005 Clinical finding 404684003 Central nervous system finding 246556002 Finding of brain 299718000 Seizure 91175000 Seizure disorder 128613002 Epilepsy 84757009 Benign familial neonatal-infantile seizures 1231282002 |
| ancestors | sorted most to least specific
|
| cpt crosswalks | |
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