Craniomicromelic syndrome 725098001
SNOMED CT code
SNOMED code | 725098001 |
---|---|
name | Craniomicromelic syndrome |
status | active |
date introduced | 2017-07-31 |
fully specified name(s) | Craniomicromelic syndrome (disorder) |
synonyms | Craniomicromelic syndrome |
attributes - group2 | |
Associated morphology | Morphologically abnormal structure 49755003 |
Finding site | Limb structure 66019005 |
Pathological process | Pathological developmental process 308490002 |
Occurrence | Congenital 255399007 |
attributes - group3 | |
Occurrence | Congenital 255399007 |
Pathological process | Pathological developmental process 308490002 |
Associated morphology | Morphologically abnormal structure 49755003 |
Finding site | Face structure 89545001 |
attributes - group1 | |
Pathological process | Pathological developmental process 308490002 |
Occurrence | Congenital 255399007 |
Finding site | Joint structure of suture of skull 51863000 |
Associated morphology | Congenital premature fusion 67798003 |
parents | |
hierarchies | a selection of possible paths SNOMED CT Concept 138875005Clinical finding 404684003 Finding of limb structure 302293008 Disorder of limb 128605003 Congenital anomaly of limb 60475009 Multiple malformation syndrome with facial-limb defects as major feature 23359005 Craniomicromelic syndrome 725098001 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Developmental disorder 5294002 Developmental hereditary disorder 363070008 Craniomicromelic syndrome 725098001 SNOMED CT Concept 138875005 Clinical finding 404684003 Musculoskeletal finding 106028002 Disorder of musculoskeletal system 928000 Hereditary disorder of musculoskeletal system 363212003 Craniomicromelic syndrome 725098001 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 Craniomicromelic syndrome 725098001 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Genetic disease 782964007 Hereditary disease 32895009 Autosomal hereditary disorder 1899006 Autosomal recessive hereditary disorder 85995004 Craniomicromelic syndrome 725098001 |
ancestors | sorted most to least specific
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cpt crosswalks |
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