Autosomal dominant rhegmatogenous retinal detachment 773727009
SNOMED CT code
| SNOMED code | 773727009 |
|---|---|
| name | Autosomal dominant rhegmatogenous retinal detachment |
| status | active |
| date introduced | 2019-01-31 |
| fully specified name(s) | Autosomal dominant rhegmatogenous retinal detachment (disorder) |
| synonyms | Autosomal dominant rhegmatogenous retinal detachment |
| attributes - group1 | |
| Finding site | Retinal structure 5665001 |
| Associated morphology | Separation 16640008 |
| attributes - group2 | |
| Due to | Break of retina 1275615004 |
| 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 Autosomal dominant rhegmatogenous retinal detachment 773727009 SNOMED CT Concept 138875005 Clinical finding 404684003 Eye / vision finding 118235002 Globe finding 246915008 Retina finding 399858007 Retinal disorder 29555009 Lesion of retina 1275616003 Retinal detachment 42059000 Rhegmatogenous retinal detachment 19620000 Autosomal dominant rhegmatogenous retinal detachment 773727009 SNOMED CT Concept 138875005 Clinical finding 404684003 Eye / vision finding 118235002 Visual system disorder 128127008 Hereditary disorder of the visual system 363343008 Autosomal dominant rhegmatogenous retinal detachment 773727009 |
| ancestors | sorted most to least specific
|
| cpt crosswalks | |
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