Epoophoron 263993001
SNOMED CT code
SNOMED code | 263993001 |
---|---|
name | Epoophoron |
status | active |
date introduced | 2002-01-31 |
fully specified name(s) | Epoophoron (disorder) |
synonyms | Epoophoron |
attributes - group1 | |
Pathological process | Pathological developmental process 308490002 |
Occurrence | Congenital 255399007 |
Associated morphology | Persistent embryonic structure 31807009 |
Finding site | Epoophoron 699003003 |
parents | |
children | |
hierarchies | a selection of possible paths SNOMED CT Concept 138875005Clinical finding 404684003 Disease 64572001 Developmental disorder 5294002 Congenital malformation 276654001 Embryological remnant 276752006 Epoophoron 263993001 SNOMED CT Concept 138875005 Clinical finding 404684003 Finding of trunk structure 302292003 Disorder of trunk 128121009 Congenital anomaly of trunk 78626001 Congenital anomaly of lower trunk 363030001 Congenital anomaly of the pelvis 47583008 Epoophoron 263993001 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Disorder of embryonic structure 609521009 Epoophoron 263993001 |
ancestors | sorted most to least specific
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cpt crosswalks |
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