SIX2-related frontonasal dysplasia 1172632008
SNOMED CT code
| SNOMED code | 1172632008 |
|---|---|
| name | SIX2-related frontonasal dysplasia |
| status | active |
| date introduced | 2021-09-30 |
| fully specified name(s) | SIX homeobox 2-related frontonasal dysplasia (disorder) |
| synonyms |
|
| attributes - group1 | |
| Occurrence | Congenital 255399007 |
| Finding site | Bone structure of cranium 89546000 |
| Associated morphology | Dysplasia 25723000 |
| Pathological process | Pathological developmental process 308490002 |
| attributes - group2 | |
| Occurrence | Congenital 255399007 |
| Finding site | Face structure 89545001 |
| Associated morphology | Morphologically abnormal structure 49755003 |
| Pathological process | Pathological developmental process 308490002 |
| parents | |
| hierarchies | a selection of possible paths SNOMED CT Concept 138875005Clinical finding 404684003 Disease 64572001 Genetic disease 782964007 Hereditary disease 32895009 Autosomal hereditary disorder 1899006 Autosomal dominant hereditary disorder 11164009 SIX2-related frontonasal dysplasia 1172632008 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Developmental disorder 5294002 Developmental hereditary disorder 363070008 SIX2-related frontonasal dysplasia 1172632008 SNOMED CT Concept 138875005 Clinical finding 404684003 Musculoskeletal finding 106028002 Disorder of musculoskeletal system 928000 Hereditary disorder of musculoskeletal system 363212003 SIX2-related frontonasal dysplasia 1172632008 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Disorder of head 118934005 Disorder of face 118930001 Congenital anomaly of face 398302004 Multiple malformation syndrome with facial defects as major feature 65094009 Frontonasal dysplasia sequence 86610004 SIX2-related frontonasal dysplasia 1172632008 |
| ancestors | sorted most to least specific
|
| cpt crosswalks | |
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