Ocular motor apraxia Cogan type 405809000
SNOMED CT code
| SNOMED code | 405809000 |
|---|---|
| name | Ocular motor apraxia Cogan type |
| status | active |
| date introduced | 2004-01-31 |
| fully specified name(s) | Ocular motor apraxia Cogan type (disorder) |
| synonyms |
|
| attributes - group1 | |
| Occurrence | Congenital 255399007 |
| Associated morphology | Morphologically abnormal structure 49755003 |
| Pathological process | Pathological developmental process 308490002 |
| Finding site | Visual structure 49549006 |
| parents | |
| children | Cortical paralysis of fixation syndrome 20485009 removed: 2018-07-31 |
| 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 Ocular motor apraxia Cogan type 405809000 SNOMED CT Concept 138875005 Clinical finding 404684003 Eye / vision finding 118235002 Visual system disorder 128127008 Disorder of eye movements 45030009 Strabismus 22066006 Oculomotor apraxia 193662007 Ocular motor apraxia Cogan type 405809000 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Developmental disorder 5294002 Developmental hereditary disorder 363070008 Ocular motor apraxia Cogan type 405809000 SNOMED CT Concept 138875005 Clinical finding 404684003 Eye / vision finding 118235002 Visual system disorder 128127008 Hereditary disorder of the visual system 363343008 Ocular motor apraxia Cogan type 405809000 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Genetic disease 782964007 Hereditary disease 32895009 Autosomal hereditary disorder 1899006 Autosomal recessive hereditary disorder 85995004 Ocular motor apraxia Cogan type 405809000 |
| ancestors | sorted most to least specific
|
| cpt crosswalks | |
Thank you for choosing Find-A-Code, please Sign In to remove ads.
Quick, Current, Complete - www.findacode.com