Congenital nuclear ophthalmoplegia 230530003
SNOMED CT code
| SNOMED code | 230530003 |
|---|---|
| name | Congenital nuclear ophthalmoplegia |
| status | active |
| date introduced | 2002-01-31 |
| fully specified name(s) | Congenital nuclear ophthalmoplegia (disorder) |
| synonyms | Congenital nuclear ophthalmoplegia |
| attributes - group1 | |
| Occurrence | Congenital 255399007 |
| Pathological process | Pathological developmental process 308490002 |
| Associated morphology | Morphologically abnormal structure 49755003 |
| Finding site | Medial longitudinal fasciculus structure 28390009 |
| attributes - group2 | |
| Finding site | Eyelid structure 80243003 |
| Pathological process | Pathological developmental process 308490002 |
| Associated morphology | Morphologically abnormal structure 49755003 |
| Occurrence | Congenital 255399007 |
| attributes - group4 | |
| Interprets | Movement 255324009 |
| attributes - group3 | |
| Interprets | Movement observable 363847004 |
| Has interpretation | Absent 2667000 |
| parents | |
| children | Ophthalmoplegia, intellectual disability, lingua scrotalis syndrome 782945001 |
| hierarchies | a selection of possible paths SNOMED CT Concept 138875005Clinical finding 404684003 Finding of movement 298325004 Movement disorder 60342002 Paralytic syndrome 29426003 Ophthalmoplegia 16110005 Congenital nuclear ophthalmoplegia 230530003 SNOMED CT Concept 138875005 Clinical finding 404684003 Central nervous system finding 246556002 Disorder of the central nervous system 23853001 Congenital anomaly of central nervous system 128124001 Congenital anomaly of brain 57148006 Dysgenesis of the brainstem 253180007 Congenital nuclear ophthalmoplegia 230530003 SNOMED CT Concept 138875005 Clinical finding 404684003 Eye / vision finding 118235002 Eyelid finding 246812007 Disorder of eyelid 60113004 Congenital anomaly of eyelid 91158006 Congenital nuclear ophthalmoplegia 230530003 SNOMED CT Concept 138875005 Clinical finding 404684003 Central nervous system finding 246556002 Finding of brain 299718000 Disorder of brain 81308009 Disorder of brain stem 95640005 Disorder of midbrain 95641009 Congenital nuclear ophthalmoplegia 230530003 |
| ancestors | sorted most to least specific
|
| cpt crosswalks | |
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