Oculootoradial syndrome 722019000
SNOMED CT code
| SNOMED code | 722019000 |
|---|---|
| name | Oculootoradial syndrome |
| status | active |
| date introduced | 2017-01-31 |
| fully specified name(s) | Oculootoradial syndrome (disorder) |
| synonyms |
|
| attributes - group1 | |
| Occurrence | Congenital 255399007 |
| Finding site | Bone structure of upper limb 371195002 |
| Pathological process | Pathological developmental process 308490002 |
| Associated morphology | Dysplasia 25723000 |
| attributes - group3 | |
| Has interpretation | Impaired 260379002 |
| Interprets | Hearing 47078008 |
| attributes - group2 | |
| Occurrence | Congenital 255399007 |
| Finding site | Right ear structure 25577004 |
| attributes - group4 | |
| Finding site | Left ear structure 89644007 |
| Occurrence | Congenital 255399007 |
| parents |
|
| hierarchies | a selection of possible paths SNOMED CT Concept 138875005Clinical finding 404684003 Disease 64572001 Developmental disorder 5294002 Disorder of bone development 371521007 Congenital anomaly of skeletal bone 8447006 Dysostosis 109420003 Oculootoradial syndrome 722019000 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Genetic disease 782964007 Hereditary disease 32895009 Autosomal hereditary disorder 1899006 Autosomal dominant hereditary disorder 11164009 Oculootoradial syndrome 722019000 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Disorder of sensory organ 1279550006 Disorder of ear 25906001 Disorder of right ear 1091281000119101 Mixed conductive and sensorineural hearing loss of right ear 18711000119105 Mixed conductive and sensorineural hearing loss, bilateral 194429000 Oculootoradial syndrome 722019000 SNOMED CT Concept 138875005 Clinical finding 404684003 Functional finding 118228005 Hearing finding 118230007 Hearing disorder 128540005 Hearing loss 15188001 Hearing loss associated with syndrome 232333009 Oculootoradial syndrome 722019000 SNOMED CT Concept 138875005 Clinical finding 404684003 Finding of limb structure 302293008 Finding of upper limb 116307009 Finding of bone of upper limb 298756009 Oculootoradial syndrome 722019000 SNOMED CT Concept 138875005 Clinical finding 404684003 Ear and auditory finding 118236001 Disorder of auditory system 362966006 Auditory system hereditary disorder 362991006 Oculootoradial syndrome 722019000 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Developmental disorder 5294002 Developmental hereditary disorder 363070008 Oculootoradial syndrome 722019000 SNOMED CT Concept 138875005 Clinical finding 404684003 Musculoskeletal finding 106028002 Disorder of musculoskeletal system 928000 Hereditary disorder of musculoskeletal system 363212003 Oculootoradial syndrome 722019000 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Developmental disorder 5294002 Congenital malformation 276654001 Congenital malformation syndrome 400038003 Multiple system malformation syndrome 82354003 Multiple malformation syndrome with limb defect as major feature 41443008 Oculootoradial syndrome 722019000 SNOMED CT Concept 138875005 Clinical finding 404684003 Finding of limb structure 302293008 Finding of upper limb 116307009 Disorder of upper limb 118947000 Congenital anomaly of upper limb 66510004 Oculootoradial syndrome 722019000 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Congenital disease 66091009 Congenital hearing disorder 95827002 Congenital sensorineural hearing loss 700453005 Congenital mixed conductive and sensorineural hearing loss 737377004 Oculootoradial syndrome 722019000 SNOMED CT Concept 138875005 Clinical finding 404684003 Finding of limb structure 302293008 Disorder of limb 128605003 Congenital anomaly of limb 60475009 Congenital dysplasia of limb 88631000119105 Oculootoradial syndrome 722019000 |
| ancestors | sorted most to least specific
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| cpt crosswalks | |
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