Hunter McAlpine craniosynostosis syndrome 721227001
SNOMED CT code
SNOMED code | 721227001 |
---|---|
name | Hunter McAlpine craniosynostosis syndrome |
status | active |
date introduced | 2017-01-31 |
fully specified name(s) | Hunter McAlpine craniosynostosis syndrome (disorder) |
synonyms | Hunter McAlpine craniosynostosis syndrome |
attributes - group1 | |
Occurrence | Congenital 255399007 |
Associated morphology | Congenital premature fusion 67798003 |
Pathological process | Pathological developmental process 308490002 |
Finding site | Joint structure of suture of skull 51863000 |
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 Hunter McAlpine craniosynostosis syndrome 721227001 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Developmental disorder 5294002 Developmental hereditary disorder 363070008 Hunter McAlpine craniosynostosis syndrome 721227001 SNOMED CT Concept 138875005 Clinical finding 404684003 Musculoskeletal finding 106028002 Disorder of musculoskeletal system 928000 Hereditary disorder of musculoskeletal system 363212003 Hunter McAlpine craniosynostosis syndrome 721227001 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 Hunter McAlpine craniosynostosis syndrome 721227001 |
ancestors | sorted most to least specific
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cpt crosswalks |
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