Congenital absence of basisphenoid bone 91871006
SNOMED CT code
| SNOMED code | 91871006 |
|---|---|
| name | Congenital absence of basisphenoid bone |
| status | active |
| date introduced | 2002-01-31 |
| fully specified name(s) | Congenital absence of basisphenoid bone (disorder) |
| synonyms |
|
| attributes - group1 | |
| Pathological process | Pathological developmental process 308490002 |
| Associated morphology | Agenesis 782173000 |
| Finding site | Entire basisphenoid bone 95945003 |
| Occurrence | Congenital 255399007 |
| parents | |
| hierarchies | a selection of possible paths SNOMED CT Concept 138875005Clinical finding 404684003 Musculoskeletal finding 106028002 Bone finding 118953000 Bone absent 298350001 Congenital absence of skeletal bone 127328006 Congenital absence of basisphenoid bone 91871006 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Disorder of head 118934005 Congenital anomaly of head 87290003 Congenital abnormality of skull and face bones 268239009 Congenital absence of basisphenoid bone 91871006 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Disorder of embryonic structure 609521009 Congenital anomaly of fetal head bones 93003001 Congenital anomaly of basisphenoid bone 92996006 Congenital absence of basisphenoid bone 91871006 |
| ancestors | sorted most to least specific
|
| cpt crosswalks | |
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