Werdnig-Hoffmann disease 64383006
SNOMED CT code
| SNOMED code | 64383006 |
|---|---|
| name | Werdnig-Hoffmann disease |
| status | active |
| date introduced | 2002-01-31 |
| fully specified name(s) | Werdnig-Hoffmann disease (disorder) |
| synonyms |
|
| attributes - group1 | |
| Finding site | Nervous system structure 25087005 |
| parents | |
| hierarchies | a selection of possible paths SNOMED CT Concept 138875005Clinical finding 404684003 Disease 64572001 Disorder of body system 362965005 Disorder of nervous system 118940003 Hereditary disorder of nervous system 363235000 Hereditary motor neuron disease 49793008 Spinal muscular atrophy 5262007 Werdnig-Hoffmann disease 64383006 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Disorder of body system 362965005 Disorder of nervous system 118940003 Motor neuron disease 37340000 Lower motor neuron disease 84590007 Anterior horn cell disease 85672005 Werdnig-Hoffmann disease 64383006 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Genetic disease 782964007 Hereditary disease 32895009 Autosomal hereditary disorder 1899006 Autosomal recessive hereditary disorder 85995004 Werdnig-Hoffmann disease 64383006 |
| ancestors | sorted most to least specific
|
| cpt crosswalks | |
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