Oculoauricular syndrome Schorderet type 763815000
SNOMED CT code
| SNOMED code | 763815000 |
|---|---|
| name | Oculoauricular syndrome Schorderet type |
| status | active |
| date introduced | 2018-07-31 |
| fully specified name(s) | Oculoauricular syndrome Schorderet type (disorder) |
| synonyms | Oculoauricular syndrome Schorderet type |
| attributes - group1 | |
| Pathological process | Pathological developmental process 308490002 |
| Associated morphology | Morphologically abnormal structure 49755003 |
| Occurrence | Congenital 255399007 |
| Finding site | External ear structure 28347008 |
| attributes - group2 | |
| Pathological process | Pathological developmental process 308490002 |
| Associated morphology | Morphologically abnormal structure 49755003 |
| Occurrence | Congenital 255399007 |
| Finding site | Eye structure 81745001 |
| 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 Oculoauricular syndrome Schorderet type 763815000 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Disorder of sensory organ 1279550006 Disorder of ear 25906001 Congenital malformation of ear 275259005 Congenital abnormality of external ear 282038006 Oculoauricular syndrome Schorderet type 763815000 SNOMED CT Concept 138875005 Clinical finding 404684003 Ear and auditory finding 118236001 Disorder of auditory system 362966006 Auditory system hereditary disorder 362991006 Oculoauricular syndrome Schorderet type 763815000 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Developmental disorder 5294002 Developmental hereditary disorder 363070008 Oculoauricular syndrome Schorderet type 763815000 SNOMED CT Concept 138875005 Clinical finding 404684003 Eye / vision finding 118235002 Visual system disorder 128127008 Hereditary disorder of the visual system 363343008 Oculoauricular syndrome Schorderet type 763815000 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Developmental disorder 5294002 Congenital malformation 276654001 Congenital malformation syndrome 400038003 Multiple system malformation syndrome 82354003 Oculoauricular syndrome Schorderet type 763815000 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Genetic disease 782964007 Hereditary disease 32895009 Autosomal hereditary disorder 1899006 Autosomal recessive hereditary disorder 85995004 Oculoauricular syndrome Schorderet type 763815000 |
| ancestors | sorted most to least specific
|
| cpt crosswalks | |
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