Albinotic fundus 55819001
SNOMED CT code
| SNOMED code | 55819001 |
|---|---|
| name | Albinotic fundus |
| status | active |
| date introduced | 2002-01-31 |
| fully specified name(s) | Albinotic fundus (disorder) |
| synonyms |
|
| attributes - group1 | |
| Pathological process | Pathological developmental process 308490002 |
| Associated morphology | Hypopigmentation 89031001 |
| Occurrence | Congenital 255399007 |
| Finding site | Structure of fundus of eye 65784005 |
| parents | |
| hierarchies | a selection of possible paths SNOMED CT Concept 138875005Clinical finding 404684003 Eye / vision finding 118235002 Globe finding 246915008 Retina finding 399858007 Retinal disorder 29555009 Lesion of retina 1275616003 Albinotic fundus 55819001 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Developmental disorder 5294002 Developmental hereditary disorder 363070008 Albinotic fundus 55819001 SNOMED CT Concept 138875005 Clinical finding 404684003 Eye / vision finding 118235002 Visual system disorder 128127008 Hereditary disorder of the visual system 363343008 Albinotic fundus 55819001 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Disorder of pigmentation 414032001 Albinotic fundus 55819001 SNOMED CT Concept 138875005 Clinical finding 404684003 Eye / vision finding 118235002 Globe finding 246915008 Retina finding 399858007 Retinal disorder 29555009 Congenital anomaly of retina 49381001 Albinotic fundus 55819001 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Genetic disease 782964007 Hereditary disease 32895009 Autosomal hereditary disorder 1899006 Autosomal recessive hereditary disorder 85995004 Albinotic fundus 55819001 |
| ancestors | sorted most to least specific
|
| cpt crosswalks | |
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