Oculootodental syndrome 770944002
SNOMED CT code
| SNOMED code | 770944002 |
|---|---|
| name | Oculootodental syndrome |
| status | active |
| date introduced | 2019-01-31 |
| fully specified name(s) | Oculootodental syndrome (disorder) |
| synonyms | Oculootodental syndrome |
| attributes - group1 | |
| Pathological process | Pathological developmental process 308490002 |
| Associated morphology | Partial monosomy 371169004 |
| Finding site | Chromosome pair 11 16312006 |
| Occurrence | Congenital 255399007 |
| attributes - group3 | |
| Pathological process | Pathological developmental process 308490002 |
| Occurrence | Congenital 255399007 |
| Finding site | Ear structure 117590005 |
| attributes - group2 | |
| Pathological process | Pathological developmental process 308490002 |
| Occurrence | Congenital 255399007 |
| Finding site | Long arm of chromosome 312242007 |
| Associated morphology | Partial monosomy 371169004 |
| attributes - group4 | |
| Pathological process | Pathological developmental process 308490002 |
| Associated morphology | Enlargement 442021009 |
| Finding site | Tooth structure 38199008 |
| attributes - group5 | |
| Interprets | Hearing 47078008 |
| 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 Oculootodental syndrome 770944002 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Disorder of sensory organ 1279550006 Disorder of ear 25906001 Oculootodental syndrome 770944002 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Developmental disorder 5294002 Congenital malformation 276654001 Oculootodental syndrome 770944002 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Congenital disease 66091009 Congenital hearing disorder 95827002 Congenital sensorineural hearing loss 700453005 Oculootodental syndrome 770944002 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Developmental disorder 5294002 Disorder of tooth development 371136004 Malformation of tooth 422775003 Macrodontia 71485000 Globodontia 707310009 Oculootodental syndrome 770944002 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Chromosomal disorder 409709004 Congenital chromosomal disease 74345006 Anomaly of chromosome pair 362984008 Anomaly of chromosome pair 11 60891003 Deletion of part of chromosome 11 726381002 Oculootodental syndrome 770944002 |
| ancestors | sorted most to least specific
|
| cpt crosswalks | |
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