Congenital velopharyngeal incompetence 427791009
SNOMED CT code
| SNOMED code | 427791009 |
|---|---|
| name | Congenital velopharyngeal incompetence |
| status | active |
| date introduced | 2008-01-31 |
| fully specified name(s) | Congenital incomplete closure of velopharyngeal apparatus due to neuromuscular dysfunction (disorder) |
| synonyms |
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| attributes - group1 | |
| Pathological process | Pathological developmental process 308490002 |
| Occurrence | Congenital 255399007 |
| Finding site | Muscle structure of pharynx 60494004 |
| parents | |
| hierarchies | a selection of possible paths SNOMED CT Concept 138875005Clinical finding 404684003 Muscle finding 106030000 Disorder of muscle 129565002 Disorder of skeletal muscle 75047002 Velopharyngeal dysfunction 229727006 Velopharyngeal incompetence 232416001 Congenital velopharyngeal incompetence 427791009 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Developmental disorder 5294002 Congenital velopharyngeal dysfunction 700285006 Congenital velopharyngeal incompetence 427791009 |
| ancestors | sorted most to least specific
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| cpt crosswalks | |
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