Anophthalmia plus syndrome 720496006
SNOMED CT code
| SNOMED code | 720496006 |
|---|---|
| name | Anophthalmia plus syndrome |
| status | active |
| date introduced | 2017-01-31 |
| fully specified name(s) | Anophthalmia plus syndrome (disorder) |
| synonyms |
|
| attributes - group2 | |
| Pathological process | Pathological developmental process 308490002 |
| Associated morphology | Absence 418560003 |
| Finding site | Entire eye proper 1290040004 |
| Occurrence | Congenital 255399007 |
| attributes - group1 | |
| Finding site | Face structure 89545001 |
| Occurrence | Congenital 255399007 |
| Pathological process | Pathological developmental process 308490002 |
| Associated morphology | Morphologically abnormal structure 49755003 |
| parents | |
| hierarchies | a selection of possible paths SNOMED CT Concept 138875005Clinical finding 404684003 Eye / vision finding 118235002 Visual system disorder 128127008 Congenital anomaly of visual system 127329003 Congenital anomaly of eye 19416009 Anophthalmia plus syndrome 720496006 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Developmental disorder 5294002 Developmental hereditary disorder 363070008 Anophthalmia plus syndrome 720496006 SNOMED CT Concept 138875005 Clinical finding 404684003 Eye / vision finding 118235002 Visual system disorder 128127008 Hereditary disorder of the visual system 363343008 Anophthalmia plus syndrome 720496006 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Disorder of head 118934005 Disorder of face 118930001 Congenital anomaly of face 398302004 Multiple malformation syndrome with facial defects as major feature 65094009 Anophthalmia plus syndrome 720496006 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Genetic disease 782964007 Hereditary disease 32895009 Autosomal hereditary disorder 1899006 Autosomal recessive hereditary disorder 85995004 Anophthalmia plus syndrome 720496006 |
| ancestors | sorted most to least specific
|
| cpt crosswalks | |
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