Epileptic encephalopathy with global cerebral demyelination 726702005
SNOMED CT code
| SNOMED code | 726702005 |
|---|---|
| name | Epileptic encephalopathy with global cerebral demyelination |
| status | active |
| date introduced | 2017-07-31 |
| fully specified name(s) | Epileptic encephalopathy with global cerebral demyelination (disorder) |
| synonyms |
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| attributes - group1 | |
| Occurrence | Congenital 255399007 |
| Associated morphology | Hypomyelination 111007000 |
| Finding site | Cerebrum 83678007 |
| Pathological process | Pathological developmental process 308490002 |
| parents | |
| hierarchies | a selection of possible paths SNOMED CT Concept 138875005Clinical finding 404684003 Disease 64572001 Developmental disorder 5294002 Neurodevelopmental disorder 700364009 Developmental and epileptic encephalopathy 1275631007 Epileptic encephalopathy with global cerebral demyelination 726702005 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Metabolic disease 75934005 Mitochondrial cytopathy 240096000 Epileptic encephalopathy with global cerebral demyelination 726702005 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Developmental disorder 5294002 Developmental hereditary disorder 363070008 Epileptic encephalopathy with global cerebral demyelination 726702005 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 Epileptic encephalopathy with global cerebral demyelination 726702005 SNOMED CT Concept 138875005 Clinical finding 404684003 Central nervous system finding 246556002 Disorder of the central nervous system 23853001 Congenital anomaly of central nervous system 128124001 Congenital anomaly of brain 57148006 Congenital anomaly of cerebrum 702628006 Epileptic encephalopathy with global cerebral demyelination 726702005 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Genetic disease 782964007 Hereditary disease 32895009 Autosomal hereditary disorder 1899006 Autosomal recessive hereditary disorder 85995004 Epileptic encephalopathy with global cerebral demyelination 726702005 |
| ancestors | sorted most to least specific
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| cpt crosswalks | |
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