Neuroferritinopathy 699299001
SNOMED CT code
| SNOMED code | 699299001 |
|---|---|
| name | Neuroferritinopathy |
| status | active |
| date introduced | 2014-01-31 |
| fully specified name(s) | Neuroferritinopathy (disorder) |
| synonyms |
|
| attributes - group2 | |
| Finding site | Basal ganglion structure 32610002 |
| attributes - group1 | |
| Causative agent | Iron and/or iron compound 767270007 |
| 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 Neuroferritinopathy 699299001 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 Neuroferritinopathy 699299001 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Metabolic disease 75934005 Disorder of mineral metabolism 45744005 Disorder of iron metabolism 30913008 Iron overload 60737008 Neuroferritinopathy 699299001 SNOMED CT Concept 138875005 Clinical finding 404684003 Finding of head and neck region 118254002 Head finding 406122000 Finding of head region 298364001 Disorder of basal ganglia 70835005 Neuroferritinopathy 699299001 |
| ancestors | sorted most to least specific
|
| cpt crosswalks | |
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