Maffucci syndrome 46041001
SNOMED CT code
SNOMED code | 46041001 |
---|---|
name | Maffucci syndrome |
status | active |
date introduced | 2002-01-31 |
fully specified name(s) | Maffucci syndrome (disorder) |
synonyms |
|
attributes - group3 | |
Pathological process | Pathological developmental process 308490002 |
Occurrence | Congenital 255399007 |
Associated morphology | Dysplasia 25723000 |
Finding site | Bone structure 272673000 |
attributes - group1 | |
Occurrence | Congenital 255399007 |
Associated morphology | Benign hemangioma 253053003 |
Finding site | Vascular structure 59820001 |
attributes - group5 | |
Associated morphology | Dysplasia 25723000 |
Finding site | Cartilage structure 771314001 |
Pathological process | Pathological developmental process 308490002 |
Occurrence | Congenital 255399007 |
parents |
|
hierarchies | a selection of possible paths SNOMED CT Concept 138875005Clinical finding 404684003 Musculoskeletal finding 106028002 Cartilage finding 118954006 Cartilage disorder 50927007 Osteochondropathy 77881008 Enchondromatosis 268274005 Maffucci syndrome 46041001 SNOMED CT Concept 138875005 Clinical finding 404684003 Cardiovascular finding 106063007 Mass of cardiovascular structure 300852003 Neoplasm of cardiovascular system 721573003 Congenital hemangioma 32361000119104 Maffucci syndrome 46041001 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Genetic disease 782964007 Maffucci syndrome 46041001 |
ancestors | sorted most to least specific
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cpt crosswalks |
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