Microcornea, myopic chorioretinal atrophy, telecanthus syndrome 774212003
SNOMED CT code
| SNOMED code | 774212003 |
|---|---|
| name | Microcornea, myopic chorioretinal atrophy, telecanthus syndrome |
| status | active |
| date introduced | 2019-01-31 |
| fully specified name(s) | Microcornea, myopic chorioretinal atrophy, telecanthus syndrome (disorder) |
| synonyms |
|
| attributes - group1 | |
| Finding site | Corneal structure 28726007 |
| Associated morphology | Congenital smallness 41086002 |
| Pathological process | Pathological developmental process 308490002 |
| Occurrence | Congenital 255399007 |
| attributes - group3 | |
| Finding site | Choroidal structure 68703001 |
| Associated morphology | Atrophy 13331008 |
| attributes - group2 | |
| Associated morphology | Atrophy 13331008 |
| Finding site | Retinal structure 5665001 |
| parents | |
| hierarchies | a selection of possible paths SNOMED CT Concept 138875005Clinical finding 404684003 Disease 64572001 Disorder of sensory organ 1279550006 Disorder of eye 371405004 Disorder of anterior segment of eye 128535002 Disorder of cornea 15250008 Congenital anomaly of cornea 128352002 Microcornea 26098002 Microcornea, myopic chorioretinal atrophy, telecanthus syndrome 774212003 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Developmental disorder 5294002 Developmental hereditary disorder 363070008 Microcornea, myopic chorioretinal atrophy, telecanthus syndrome 774212003 SNOMED CT Concept 138875005 Clinical finding 404684003 Eye / vision finding 118235002 Visual system disorder 128127008 Hereditary disorder of the visual system 363343008 Microcornea, myopic chorioretinal atrophy, telecanthus syndrome 774212003 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Developmental disorder 5294002 Congenital malformation 276654001 Congenital malformation syndrome 400038003 Microcornea, myopic chorioretinal atrophy, telecanthus syndrome 774212003 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Genetic disease 782964007 Hereditary disease 32895009 Autosomal hereditary disorder 1899006 Autosomal recessive hereditary disorder 85995004 Microcornea, myopic chorioretinal atrophy, telecanthus syndrome 774212003 SNOMED CT Concept 138875005 Clinical finding 404684003 Eye / vision finding 118235002 Globe finding 246915008 Choroid finding 247195001 Choroidal atrophy 247200005 Chorioretinal atrophy 95686007 Microcornea, myopic chorioretinal atrophy, telecanthus syndrome 774212003 |
| ancestors | sorted most to least specific
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| cpt crosswalks | |
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