EDICT syndrome 722439009
SNOMED CT code
SNOMED code | 722439009 |
---|---|
name | EDICT syndrome |
status | active |
date introduced | 2017-01-31 |
fully specified name(s) | Endothelial dystrophy, iris hypoplasia, congenital cataract, stromal thinning syndrome (disorder) |
synonyms |
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attributes - group1 | |
Associated morphology | Morphologically abnormal structure 49755003 |
Pathological process | Pathological developmental process 308490002 |
Occurrence | Congenital 255399007 |
Finding site | Anterior eyeball segment structure 32259006 |
parents | |
hierarchies | a selection of possible paths SNOMED CT Concept 138875005Clinical finding 404684003 Disease 64572001 Genetic disease 782964007 Hereditary disease 32895009 Autosomal hereditary disorder 1899006 Autosomal dominant hereditary disorder 11164009 EDICT syndrome 722439009 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Developmental disorder 5294002 Developmental hereditary disorder 363070008 EDICT syndrome 722439009 SNOMED CT Concept 138875005 Clinical finding 404684003 Eye / vision finding 118235002 Visual system disorder 128127008 Hereditary disorder of the visual system 363343008 EDICT syndrome 722439009 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Disorder of sensory organ 1279550006 Disorder of eye 371405004 Disorder of anterior segment of eye 128535002 Congenital anomaly of anterior segment of eye 429448005 EDICT syndrome 722439009 |
ancestors | sorted most to least specific
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cpt crosswalks |
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