Deafness and myopia syndrome 720506002
SNOMED CT code
| SNOMED code | 720506002 |
|---|---|
| name | Deafness and myopia syndrome |
| status | active |
| date introduced | 2017-01-31 |
| fully specified name(s) | Deafness and myopia syndrome (disorder) |
| synonyms |
|
| attributes - group3 | |
| Interprets | Hearing 47078008 |
| attributes - group2 | |
| Finding site | Visual structure 49549006 |
| attributes - group1 | |
| Finding site | Ear structure 117590005 |
| parents | |
| hierarchies | a selection of possible paths SNOMED CT Concept 138875005Clinical finding 404684003 Functional finding 118228005 Hearing finding 118230007 Hearing disorder 128540005 Hearing loss 15188001 Hearing loss associated with syndrome 232333009 Deafness and myopia syndrome 720506002 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Disorder of sensory organ 1279550006 Disorder of ear 25906001 Deafness and myopia syndrome 720506002 SNOMED CT Concept 138875005 Clinical finding 404684003 Eye / vision finding 118235002 Visual system disorder 128127008 Disorder of vision 95677002 Disorder of refraction AND/OR accommodation 72128008 Disorder of refraction 39021009 Myopia 57190000 Severe myopia 34187009 Deafness and myopia syndrome 720506002 SNOMED CT Concept 138875005 Clinical finding 404684003 Ear and auditory finding 118236001 Disorder of auditory system 362966006 Auditory system hereditary disorder 362991006 Deafness and myopia syndrome 720506002 SNOMED CT Concept 138875005 Clinical finding 404684003 Eye / vision finding 118235002 Visual system disorder 128127008 Hereditary disorder of the visual system 363343008 Deafness and myopia syndrome 720506002 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Genetic disease 782964007 Hereditary disease 32895009 Autosomal hereditary disorder 1899006 Autosomal recessive hereditary disorder 85995004 Deafness and myopia syndrome 720506002 |
| ancestors | sorted most to least specific
|
| cpt crosswalks | |
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