Congenital keratoglobus 204118005
SNOMED CT code
SNOMED code | 204118005 |
---|---|
name | Congenital keratoglobus |
status | active |
date introduced | 2002-01-31 |
fully specified name(s) | Congenital keratoglobus (disorder) |
synonyms | Congenital keratoglobus |
attributes - group2 | |
Occurrence | Congenital 255399007 |
Associated morphology | Protrusion 112639008 |
Pathological process | Pathological developmental process 308490002 |
Finding site | Corneal structure 28726007 |
attributes - group3 | |
Interprets | Corneal thickness 251691009 |
Has interpretation | Thin 18043004 |
parents | |
hierarchies | a selection of possible paths SNOMED CT Concept 138875005Clinical finding 404684003 Disease 64572001 Disorder of sensory organ 1279550006 Disorder of eye 371405004 Disorder of anterior segment of eye 128535002 Disorder of cornea 15250008 Congenital anomaly of cornea 128352002 Congenital keratoglobus 204118005 SNOMED CT Concept 138875005 Clinical finding 404684003 Corneal thinning 423459005 Keratoglobus 388840007 Congenital keratoglobus 204118005 |
ancestors | sorted most to least specific
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cpt crosswalks |
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