Reticular dystrophy of retinal pigment epithelium 723502001
SNOMED CT code
| SNOMED code | 723502001 |
|---|---|
| name | Reticular dystrophy of retinal pigment epithelium |
| status | active |
| date introduced | 2017-07-31 |
| fully specified name(s) | Reticular dystrophy of retinal pigment epithelium (disorder) |
| synonyms | Reticular dystrophy of retinal pigment epithelium |
| attributes - group1 | |
| Associated morphology | Dystrophy 4720007 |
| Finding site | Structure of retinal pigment epithelium 41275009 |
| parents |
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| 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 Reticular dystrophy of retinal pigment epithelium 723502001 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Disorder of sensory organ 1279550006 Disorder of eye 371405004 Anomaly of eye 11131000119108 Retinal pigment epithelial abnormality 421689001 Retinal pigment epithelial dystrophy 342581000119102 Reticular dystrophy of retinal pigment epithelium 723502001 SNOMED CT Concept 138875005 Clinical finding 404684003 Eye / vision finding 118235002 Visual system disorder 128127008 Hereditary disorder of the visual system 363343008 Hereditary retinal dystrophy 41799005 Reticular dystrophy of retinal pigment epithelium 723502001 |
| ancestors | sorted most to least specific
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| cpt crosswalks | |
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