SATB2-associated syndrome 1208488006
SNOMED CT code
| SNOMED code | 1208488006 |
|---|---|
| name | SATB2-associated syndrome |
| status | active |
| date introduced | 2022-03-31 |
| fully specified name(s) | Special AT-rich sequence-binding protein 2-associated syndrome (disorder) |
| synonyms |
|
| attributes - group1 | |
| Occurrence | Congenital 255399007 |
| Finding site | Tooth structure 38199008 |
| Associated morphology | Morphologically abnormal structure 49755003 |
| Pathological process | Pathological developmental process 308490002 |
| attributes - group2 | |
| Occurrence | Congenital 255399007 |
| Finding site | Bone structure of mandible 91609006 |
| Associated morphology | Hypoplasia 55199003 |
| Pathological process | Pathological developmental process 308490002 |
| attributes - group3 | |
| Interprets | Adaptation behavior 406208005 |
| Has interpretation | Impaired 260379002 |
| attributes - group4 | |
| Interprets | Intellectual ability 247573007 |
| Has interpretation | Impaired 260379002 |
| parents | |
| hierarchies | a selection of possible paths SNOMED CT Concept 138875005Clinical finding 404684003 Mental state, behavior and/or psychosocial function finding 384821006 Behavior finding 844005 Intellectual disability 110359009 SATB2-associated syndrome 1208488006 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Developmental disorder 5294002 Developmental delay 248290002 SATB2-associated syndrome 1208488006 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Disorder of head 118934005 Disorder of jaw 37156001 Congenital anomaly of jaw 95473006 Congenital anomaly of mandible 128224008 Congenital micrognathism 32958008 SATB2-associated syndrome 1208488006 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 SATB2-associated syndrome 1208488006 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 SATB2-associated syndrome 1208488006 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Genetic disease 782964007 SATB2-associated syndrome 1208488006 |
| ancestors | sorted most to least specific
|
| cpt crosswalks | |
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