Osteogenesis imperfecta type I 385482004
SNOMED CT code
SNOMED code | 385482004 |
---|---|
name | Osteogenesis imperfecta type I |
status | active |
date introduced | 2003-01-31 |
fully specified name(s) | Osteogenesis imperfecta type I (disorder) |
synonyms |
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attributes - group1 | |
Occurrence | Congenital 255399007 |
Pathological process | Pathological developmental process 308490002 |
Associated morphology | Dysplasia 25723000 |
Finding site | Bone structure 272673000 |
attributes - group2 | |
Has interpretation | Abnormal 263654008 |
Interprets | Bone formation 83323007 |
parents | |
children | |
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 Osteogenesis imperfecta type I 385482004 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Developmental disorder 5294002 Developmental hereditary disorder 363070008 Osteogenesis imperfecta type I 385482004 SNOMED CT Concept 138875005 Clinical finding 404684003 Musculoskeletal finding 106028002 Disorder of musculoskeletal system 928000 Hereditary disorder of musculoskeletal system 363212003 Osteogenesis imperfecta type I 385482004 SNOMED CT Concept 138875005 Clinical finding 404684003 Functional finding 118228005 Abnormal bone formation 36123008 Osteogenesis imperfecta 78314001 Osteogenesis imperfecta type I 385482004 |
ancestors | sorted most to least specific
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cpt crosswalks |
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