Goldmann-Favre syndrome 232065000
SNOMED CT code
| SNOMED code | 232065000 |
|---|---|
| name | Goldmann-Favre syndrome |
| status | active |
| date introduced | 2002-01-31 |
| fully specified name(s) | Goldmann-Favre syndrome (disorder) |
| synonyms |
|
| attributes - group3 | |
| Clinical course | Progressive 255314001 |
| attributes - group2 | |
| Associated morphology | Dystrophy 4720007 |
| Finding site | Retinal structure 5665001 |
| attributes - group1 | |
| Associated morphology | Dystrophy 4720007 |
| Finding site | Vitreous body structure 47538007 |
| parents | |
| hierarchies | a selection of possible paths SNOMED CT Concept 138875005Clinical finding 404684003 Disease 64572001 Chronic disease 27624003 Chronic disease of ocular adnexa 128296004 Goldmann-Favre syndrome 232065000 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Disorder of connective tissue 105969002 Connective tissue hereditary disorder 363045008 Goldmann-Favre syndrome 232065000 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Disorder of connective tissue 105969002 Disorder of vitreous body 76682005 Vitreous degeneration 60189009 Goldmann-Favre syndrome 232065000 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 Vitreoretinal dystrophy 79556007 Goldmann-Favre syndrome 232065000 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Genetic disease 782964007 Hereditary disease 32895009 Autosomal hereditary disorder 1899006 Autosomal recessive hereditary disorder 85995004 Goldmann-Favre syndrome 232065000 |
| ancestors | sorted most to least specific
|
| cpt crosswalks | |
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