Summitt syndrome 733606001
SNOMED CT code
| SNOMED code | 733606001 |
|---|---|
| name | Summitt syndrome |
| status | active |
| date introduced | 2017-07-31 |
| fully specified name(s) | Summitt syndrome (disorder) |
| synonyms |
|
| attributes - group2 | |
| Occurrence | Congenital 255399007 |
| Finding site | Digit structure 82680008 |
| Pathological process | Pathological developmental process 308490002 |
| Associated morphology | Congenital abnormal fusion 37764001 |
| attributes - group1 | |
| Finding site | Joint structure of suture of skull 51863000 |
| Occurrence | Congenital 255399007 |
| Associated morphology | Congenital premature fusion 67798003 |
| Pathological process | Pathological developmental process 308490002 |
| parents | |
| hierarchies | a selection of possible paths SNOMED CT Concept 138875005Clinical finding 404684003 Disease 64572001 Genetic disease 782964007 Acrocephalosyndactyly 268262006 Summitt syndrome 733606001 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Developmental disorder 5294002 Developmental hereditary disorder 363070008 Summitt syndrome 733606001 SNOMED CT Concept 138875005 Clinical finding 404684003 Musculoskeletal finding 106028002 Disorder of musculoskeletal system 928000 Hereditary disorder of musculoskeletal system 363212003 Summitt syndrome 733606001 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Genetic disease 782964007 Hereditary disease 32895009 Autosomal hereditary disorder 1899006 Autosomal recessive hereditary disorder 85995004 Summitt syndrome 733606001 |
| ancestors | sorted most to least specific
|
| cpt crosswalks | |
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