Congenital cochleovestibular malformation 1234911006
SNOMED CT code
| SNOMED code | 1234911006 |
|---|---|
| name | Congenital cochleovestibular malformation |
| status | active |
| date introduced | 2022-07-31 |
| fully specified name(s) | Congenital cochleovestibular malformation (disorder) |
| synonyms | Congenital cochleovestibular malformation |
| attributes - group2 | |
| Interprets | Hearing 47078008 |
| Has interpretation | Decreased 1250004 |
| attributes - group1 | |
| Occurrence | Congenital 255399007 |
| Finding site | Inner ear structure 22945000 |
| Associated morphology | Morphologically abnormal structure 49755003 |
| Pathological process | Pathological developmental process 308490002 |
| parents | |
| hierarchies | a selection of possible paths SNOMED CT Concept 138875005Clinical finding 404684003 Functional finding 118228005 Hearing finding 118230007 Decreased hearing 103276001 Congenital cochleovestibular malformation 1234911006 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Congenital disease 66091009 Congenital hearing disorder 95827002 Congenital anomaly of ear with impairment of hearing 111339003 Congenital cochleovestibular malformation 1234911006 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Disorder of sensory organ 1279550006 Disorder of ear 25906001 Disorder of inner ear 232297009 Congenital anomaly of inner ear 43353004 Congenital cochleovestibular malformation 1234911006 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Congenital disease 66091009 Congenital hearing disorder 95827002 Congenital sensorineural hearing loss 700453005 Congenital cochleovestibular malformation 1234911006 |
| ancestors | sorted most to least specific
|
| cpt crosswalks | |
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