Grayson Wilbrandt corneal dystrophy 717286002
SNOMED CT code
| SNOMED code | 717286002 |
|---|---|
| name | Grayson Wilbrandt corneal dystrophy |
| status | active |
| date introduced | 2017-01-31 |
| fully specified name(s) | Grayson Wilbrandt dystrophy of cornea (disorder) |
| synonyms |
|
| attributes - group2 | |
| Finding site | Anterior limiting lamina of cornea 55143001 |
| Associated morphology | Opacity 128305008 |
| attributes - group3 | |
| Finding site | Anterior limiting lamina of cornea 55143001 |
| Associated morphology | Dystrophy 4720007 |
| 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 Grayson Wilbrandt corneal dystrophy 717286002 SNOMED CT Concept 138875005 Clinical finding 404684003 Eye / vision finding 118235002 Globe finding 246915008 Anterior segment finding 418727003 Corneal finding 246924004 Bowman's membrane finding 246952008 Grayson Wilbrandt corneal dystrophy 717286002 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Degenerative disorder 362975008 Degenerative disorder of eye 62585004 Corneal degeneration 111521006 Corneal opacity 64634000 Grayson Wilbrandt corneal dystrophy 717286002 SNOMED CT Concept 138875005 Clinical finding 404684003 Eye / vision finding 118235002 Visual system disorder 128127008 Hereditary disorder of the visual system 363343008 Hereditary corneal dystrophy 77797009 Grayson Wilbrandt corneal dystrophy 717286002 |
| ancestors | sorted most to least specific
|
| cpt crosswalks | |
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