Catel Manzke syndrome 722383001
SNOMED CT code
SNOMED code | 722383001 |
---|---|
name | Catel Manzke syndrome |
status | active |
date introduced | 2017-01-31 |
fully specified name(s) | Catel Manzke syndrome (disorder) |
synonyms |
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attributes - group1 | |
Occurrence | Congenital 255399007 |
Pathological process | Pathological developmental process 308490002 |
Finding site | Bone structure 272673000 |
Associated morphology | Dysplasia 25723000 |
attributes - group2 | |
Associated morphology | Morphologically abnormal structure 49755003 |
Pathological process | Pathological developmental process 308490002 |
Occurrence | Congenital 255399007 |
Finding site | Index finger structure 83738005 |
parents | |
hierarchies | a selection of possible paths SNOMED CT Concept 138875005Clinical finding 404684003 Disease 64572001 Developmental disorder 5294002 Disorder of bone development 371521007 Congenital anomaly of skeletal bone 8447006 Dysostosis 109420003 Catel Manzke syndrome 722383001 SNOMED CT Concept 138875005 Clinical finding 404684003 Finding of limb structure 302293008 Disorder of limb 128605003 Disorder of digit 128597007 Congenital anomaly of digit 403855001 Congenital anomaly of finger 20948006 Catel Manzke syndrome 722383001 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Developmental disorder 5294002 Developmental hereditary disorder 363070008 Catel Manzke syndrome 722383001 SNOMED CT Concept 138875005 Clinical finding 404684003 Musculoskeletal finding 106028002 Disorder of musculoskeletal system 928000 Hereditary disorder of musculoskeletal system 363212003 Catel Manzke syndrome 722383001 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Developmental disorder 5294002 Congenital malformation 276654001 Congenital malformation syndrome 400038003 Multiple system malformation syndrome 82354003 Multiple malformation syndrome with limb defect as major feature 41443008 Catel Manzke syndrome 722383001 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Genetic disease 782964007 Hereditary disease 32895009 Autosomal hereditary disorder 1899006 Autosomal recessive hereditary disorder 85995004 Catel Manzke syndrome 722383001 |
ancestors | sorted most to least specific
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cpt crosswalks |
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