Crouzon syndrome 28861008
SNOMED CT code
SNOMED code | 28861008 |
---|---|
name | Crouzon syndrome |
status | active |
date introduced | 2002-01-31 |
fully specified name(s) | Crouzon syndrome (disorder) |
synonyms |
|
attributes - group2 | |
Finding site | Joint structure of suture of skull 51863000 |
Associated morphology | Congenital premature fusion 67798003 |
Occurrence | Congenital 255399007 |
Pathological process | Pathological developmental process 308490002 |
attributes - group1 | |
Pathological process | Pathological developmental process 308490002 |
Occurrence | Congenital 255399007 |
Associated morphology | Morphologically abnormal structure 49755003 |
Finding site | Face structure 89545001 |
parents | |
children | Crouzon syndrome with acanthosis nigricans 702361006 |
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 Crouzon syndrome 28861008 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Developmental disorder 5294002 Developmental hereditary disorder 363070008 Crouzon syndrome 28861008 SNOMED CT Concept 138875005 Clinical finding 404684003 Musculoskeletal finding 106028002 Disorder of musculoskeletal system 928000 Hereditary disorder of musculoskeletal system 363212003 Crouzon syndrome 28861008 SNOMED CT Concept 138875005 Clinical finding 404684003 Musculoskeletal finding 106028002 Joint finding 118952005 Cranial suture finding 248387005 Imperfect fusion of skull 23939000 Craniosynostosis syndrome 57219006 Crouzon syndrome 28861008 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 Crouzon syndrome 28861008 |
ancestors | sorted most to least specific
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cpt crosswalks |
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