Blue cone monochromatism 789676005
SNOMED CT code
| SNOMED code | 789676005 |
|---|---|
| name | Blue cone monochromatism |
| status | active |
| date introduced | 2020-01-31 |
| fully specified name(s) | Blue cone monochromatism (disorder) |
| synonyms |
|
| attributes - group1 | |
| Occurrence | Congenital 255399007 |
| Associated morphology | Dystrophy 4720007 |
| Pathological process | Pathological developmental process 308490002 |
| Finding site | Cone of retina 67540009 |
| parents |
|
| hierarchies | a selection of possible paths SNOMED CT Concept 138875005Clinical finding 404684003 Disease 64572001 Genetic disease 782964007 Hereditary disease 32895009 Sex-linked hereditary disorder 82852009 X-linked hereditary disease 128430005 X-linked recessive hereditary disease 1162976004 Blue cone monochromatism 789676005 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Congenital disease 66091009 Congenital color blindness 232148006 Blue cone monochromatism 789676005 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 Blue cone monochromatism 789676005 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Developmental disorder 5294002 Developmental hereditary disorder 363070008 Blue cone monochromatism 789676005 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 Blue cone monochromatism 789676005 |
| ancestors | sorted most to least specific
|
| cpt crosswalks | |
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