Charlie M syndrome 733034007
SNOMED CT code
SNOMED code | 733034007 |
---|---|
name | Charlie M syndrome |
status | active |
date introduced | 2017-07-31 |
fully specified name(s) | Charlie M syndrome (disorder) |
synonyms | Charlie M syndrome |
attributes - group2 | |
Pathological process | Pathological developmental process 308490002 |
Associated morphology | Morphologically abnormal structure 49755003 |
Occurrence | Congenital 255399007 |
Finding site | Bone structure of mandible 91609006 |
attributes - group1 | |
Associated morphology | Morphologically abnormal structure 49755003 |
Occurrence | Congenital 255399007 |
Pathological process | Pathological developmental process 308490002 |
Finding site | Limb structure 66019005 |
attributes - group3 | |
Associated morphology | Morphologically abnormal structure 49755003 |
Pathological process | Pathological developmental process 308490002 |
Occurrence | Congenital 255399007 |
Finding site | Sphenoid bone structure 73117003 |
attributes - group4 | |
Pathological process | Pathological developmental process 308490002 |
Associated morphology | Morphologically abnormal structure 49755003 |
Occurrence | Congenital 255399007 |
Finding site | Structure of internal part of mouth 700016008 |
parents | |
hierarchies | a selection of possible paths SNOMED CT Concept 138875005Clinical finding 404684003 Disease 64572001 Disorder of head 118934005 Disorder of skull 118945008 Congenital anomaly of skull 51655004 Hypertelorism 22006008 Charlie M syndrome 733034007 SNOMED CT Concept 138875005 Clinical 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 Oromandibular-limb hypogenesis spectrum 89444000 Charlie M syndrome 733034007 |
ancestors | sorted most to least specific
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cpt crosswalks |
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