X-linked endothelial corneal dystrophy 718579008
SNOMED CT code
| SNOMED code | 718579008 |
|---|---|
| name | X-linked endothelial corneal dystrophy |
| status | active |
| date introduced | 2017-01-31 |
| fully specified name(s) | X-linked endothelial dystrophy of cornea (disorder) |
| synonyms |
|
| attributes - group1 | |
| Associated morphology | Dystrophy 4720007 |
| Occurrence | Congenital 255399007 |
| Finding site | Structure of corneal endothelium 65431007 |
| parents |
|
| hierarchies | a selection of possible paths SNOMED CT Concept 138875005Clinical finding 404684003 Disease 64572001 Genetic disease 782964007 Hereditary disease 32895009 Sex-linked hereditary disorder 82852009 X-linked hereditary disease 128430005 X-linked recessive hereditary disease 1162976004 X-linked endothelial corneal dystrophy 718579008 SNOMED CT Concept 138875005 Clinical finding 404684003 Eye / vision finding 118235002 Globe finding 246915008 Anterior segment finding 418727003 Corneal finding 246924004 Corneal endothelium finding 246966003 Corneal endothelial dystrophy 416960004 X-linked endothelial corneal dystrophy 718579008 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Congenital disease 66091009 X-linked endothelial corneal dystrophy 718579008 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 X-linked endothelial corneal dystrophy 718579008 |
| ancestors | sorted most to least specific
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| cpt crosswalks | |
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