Retinohepatoendocrinologic syndrome 724000006
SNOMED CT code
| SNOMED code | 724000006 |
|---|---|
| name | Retinohepatoendocrinologic syndrome |
| status | active |
| date introduced | 2017-07-31 |
| fully specified name(s) | Retinohepatoendocrinologic syndrome (disorder) |
| synonyms |
|
| attributes - group1 | |
| Associated morphology | Degenerative abnormality 107669003 |
| Finding site | Liver structure 10200004 |
| attributes - group2 | |
| Finding site | Cone of retina 67540009 |
| Associated morphology | Dystrophy 4720007 |
| attributes - group3 | |
| Finding site | Endocrine structure 113331007 |
| parents | |
| hierarchies | a selection of possible paths SNOMED CT Concept 138875005Clinical finding 404684003 Digestive system finding 386617003 Liver finding 249565005 Disease of liver 235856003 Retinohepatoendocrinologic syndrome 724000006 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 Cone dystrophy 312917007 Retinohepatoendocrinologic syndrome 724000006 SNOMED CT Concept 138875005 Clinical finding 404684003 Digestive system finding 386617003 Disorder of digestive system 53619000 Digestive system hereditary disorder 363080007 Retinohepatoendocrinologic syndrome 724000006 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Disorder of body system 362965005 Disorder of endocrine system 362969004 Hereditary disorder of endocrine system 363104002 Retinohepatoendocrinologic syndrome 724000006 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Genetic disease 782964007 Hereditary disease 32895009 Autosomal hereditary disorder 1899006 Autosomal recessive hereditary disorder 85995004 Retinohepatoendocrinologic syndrome 724000006 |
| ancestors | sorted most to least specific
|
| cpt crosswalks | |
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