Congenital deafness with labyrinthine aplasia, microtia and microdontia 702360007
SNOMED CT code
| SNOMED code | 702360007 |
|---|---|
| name | Congenital deafness with labyrinthine aplasia, microtia and microdontia |
| status | active |
| date introduced | 2014-07-31 |
| fully specified name(s) | Congenital deafness with labyrinthine aplasia, microtia and microdontia (disorder) |
| synonyms |
|
| attributes - group1 | |
| Associated morphology | Morphologically abnormal structure 49755003 |
| Occurrence | Congenital 255399007 |
| Pathological process | Pathological developmental process 308490002 |
| Finding site | Inner ear structure 22945000 |
| attributes - group3 | |
| Associated morphology | Morphologically abnormal structure 49755003 |
| Pathological process | Pathological developmental process 308490002 |
| Occurrence | Congenital 255399007 |
| Finding site | Tooth structure 38199008 |
| attributes - group5 | |
| Associated morphology | Growth alteration 57697001 |
| Finding site | Tooth structure 38199008 |
| Pathological process | Pathological developmental process 308490002 |
| attributes - group4 | |
| Interprets | Hearing 47078008 |
| attributes - group2 | |
| Pathological process | Pathological developmental process 308490002 |
| Occurrence | Congenital 255399007 |
| Finding site | External ear structure 28347008 |
| Associated morphology | Congenital smallness 41086002 |
| parents |
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| hierarchies | a selection of possible paths SNOMED CT Concept 138875005Clinical finding 404684003 Disease 64572001 Congenital disease 66091009 Congenital hearing disorder 95827002 Congenital anomaly of ear with impairment of hearing 111339003 Congenital deafness with labyrinthine aplasia, microtia and microdontia 702360007 SNOMED CT Concept 138875005 Clinical finding 404684003 Digestive system finding 386617003 Disorder of digestive system 53619000 Digestive system hereditary disorder 363080007 Hereditary disorder of tooth 1148766007 Congenital deafness with labyrinthine aplasia, microtia and microdontia 702360007 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 Congenital deafness with labyrinthine aplasia, microtia and microdontia 702360007 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Developmental disorder 5294002 Disorder of tooth development 371136004 Malformation of tooth 422775003 Microdontia 32337007 Congenital deafness with labyrinthine aplasia, microtia and microdontia 702360007 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 Microtia 35045004 Congenital deafness with labyrinthine aplasia, microtia and microdontia 702360007 SNOMED CT Concept 138875005 Clinical finding 404684003 Ear and auditory finding 118236001 Disorder of auditory system 362966006 Auditory system hereditary disorder 362991006 Congenital deafness with labyrinthine aplasia, microtia and microdontia 702360007 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Developmental disorder 5294002 Developmental hereditary disorder 363070008 Congenital deafness with labyrinthine aplasia, microtia and microdontia 702360007 SNOMED CT Concept 138875005 Clinical finding 404684003 Digestive system finding 386617003 Finding of mouth region 423066003 Oral cavity finding 116337000 Congenital abnormality of oral cavity 282041002 Congenital anomaly of tooth 422977003 Congenital deafness with labyrinthine aplasia, microtia and microdontia 702360007 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Disorder of sensory organ 1279550006 Disorder of ear 25906001 Disorder of inner ear 232297009 Congenital anomaly of inner ear 43353004 Congenital deafness with labyrinthine aplasia, microtia and microdontia 702360007 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Developmental disorder 5294002 Congenital malformation 276654001 Congenital malformation syndrome 400038003 Multiple system malformation syndrome 82354003 Congenital deafness with labyrinthine aplasia, microtia and microdontia 702360007 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Genetic disease 782964007 Hereditary disease 32895009 Autosomal hereditary disorder 1899006 Autosomal recessive hereditary disorder 85995004 Congenital deafness with labyrinthine aplasia, microtia and microdontia 702360007 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Congenital disease 66091009 Congenital hearing disorder 95827002 Congenital deafness 95828007 Congenital deafness with labyrinthine aplasia, microtia and microdontia 702360007 |
| ancestors | sorted most to least specific
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| cpt crosswalks | |
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