Vanishing white matter disease 447351004
SNOMED CT code
SNOMED code | 447351004 |
---|---|
name | Vanishing white matter disease |
status | active |
date introduced | 2011-01-31 |
fully specified name(s) | Vanishing white matter disease (disorder) |
synonyms |
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attributes - group1 | |
Associated morphology | Myelin sheath alteration 125495003 |
Finding site | Myelinated nerve fiber structure 54115001 |
attributes - group2 | |
Finding site | Cerebral white matter structure 68523003 |
Associated morphology | Dystrophy 4720007 |
parents | |
children | Ovarioleukodystrophy 1156768008 |
hierarchies | a selection of possible paths SNOMED CT Concept 138875005Clinical finding 404684003 Disease 64572001 Degenerative disorder 362975008 Degenerative disease of the central nervous system 80690008 Hereditary degenerative disease of central nervous system 106018006 Vanishing white matter disease 447351004 SNOMED CT Concept 138875005 Clinical finding 404684003 Neurological lesion 299735001 Leukodystrophy 192781003 Vanishing white matter disease 447351004 SNOMED CT Concept 138875005 Clinical finding 404684003 Finding of head and neck region 118254002 Head finding 406122000 Finding of head region 298364001 Leukoencephalopathy 22811006 Vanishing white matter disease 447351004 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Degenerative disorder 362975008 Degenerative disease of the central nervous system 80690008 Degenerative brain disorder 52522001 Cerebral degeneration 418143002 Vanishing white matter disease 447351004 SNOMED CT Concept 138875005 Clinical finding 404684003 Finding of coordination 298314008 Ataxia 20262006 Hereditary ataxia 763597000 Vanishing white matter disease 447351004 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Genetic disease 782964007 Hereditary disease 32895009 Autosomal hereditary disorder 1899006 Autosomal recessive hereditary disorder 85995004 Vanishing white matter disease 447351004 |
ancestors | sorted most to least specific
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cpt crosswalks |
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