Brown-Vialetto-Van Laere syndrome 699866005
SNOMED CT code
| SNOMED code | 699866005 |
|---|---|
| name | Brown-Vialetto-Van Laere syndrome |
| status | active |
| date introduced | 2014-01-31 |
| fully specified name(s) | Progressive bulbar palsy with sensorineural deafness (disorder) |
| synonyms |
|
| attributes - group2 | |
| Finding site | Auditory structure 91159003 |
| attributes - group3 | |
| Interprets | Hearing 47078008 |
| attributes - group1 | |
| Finding site | Structure of cranial nerve nucleus 19465004 |
| parents | |
| hierarchies | a selection of possible paths SNOMED CT Concept 138875005Clinical finding 404684003 Ear and auditory finding 118236001 Disorder of auditory system 362966006 Auditory system hereditary disorder 362991006 Brown-Vialetto-Van Laere syndrome 699866005 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 Brown-Vialetto-Van Laere syndrome 699866005 SNOMED CT Concept 138875005 Clinical finding 404684003 Finding of head and neck region 118254002 Head finding 406122000 Finding of head region 298364001 Progressive bulbar palsy 54304004 Brown-Vialetto-Van Laere syndrome 699866005 SNOMED CT Concept 138875005 Clinical finding 404684003 Functional finding 118228005 Hearing finding 118230007 Hearing disorder 128540005 Hearing loss 15188001 Sensorineural hearing loss 60700002 Brown-Vialetto-Van Laere syndrome 699866005 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Genetic disease 782964007 Hereditary disease 32895009 Autosomal hereditary disorder 1899006 Autosomal recessive hereditary disorder 85995004 Brown-Vialetto-Van Laere syndrome 699866005 |
| ancestors | sorted most to least specific
|
| cpt crosswalks | |
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