Action myoclonus renal failure syndrome 764453009
SNOMED CT code
| SNOMED code | 764453009 |
|---|---|
| name | Action myoclonus renal failure syndrome |
| status | active |
| date introduced | 2018-07-31 |
| fully specified name(s) | Action myoclonus renal failure syndrome (disorder) |
| synonyms |
|
| attributes - group1 | |
| Finding site | Brain structure 12738006 |
| Occurrence | Congenital 255399007 |
| parents | |
| hierarchies | a selection of possible paths SNOMED CT Concept 138875005Clinical finding 404684003 Central nervous system finding 246556002 Finding of brain 299718000 Seizure 91175000 Seizure disorder 128613002 Epilepsy 84757009 Progressive myoclonic epilepsy 267581004 Action myoclonus renal failure syndrome 764453009 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 Action myoclonus renal failure syndrome 764453009 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Congenital disease 66091009 Action myoclonus renal failure syndrome 764453009 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Genetic disease 782964007 Hereditary disease 32895009 Autosomal hereditary disorder 1899006 Autosomal recessive hereditary disorder 85995004 Action myoclonus renal failure syndrome 764453009 |
| ancestors | sorted most to least specific
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| cpt crosswalks | |
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