Osteogenesis imperfecta type 5 1003379004
SNOMED CT code
| SNOMED code | 1003379004 |
|---|---|
| name | Osteogenesis imperfecta type 5 |
| status | active |
| date introduced | 2021-01-31 |
| fully specified name(s) | Osteogenesis imperfecta type 5 (disorder) |
| synonyms |
|
| attributes - group1 | |
| Associated morphology | Dysplasia 25723000 |
| Occurrence | Congenital 255399007 |
| Pathological process | Pathological developmental process 308490002 |
| Finding site | Bone structure 272673000 |
| attributes - group2 | |
| Has interpretation | Abnormal 263654008 |
| Interprets | Bone formation 83323007 |
| attributes - group3 | |
| Interprets | Height / growth measure 271603002 |
| parents | |
| hierarchies | a selection of possible paths SNOMED CT Concept 138875005Clinical finding 404684003 Disease 64572001 Genetic disease 782964007 Hereditary disease 32895009 Autosomal hereditary disorder 1899006 Osteogenesis imperfecta type 5 1003379004 SNOMED CT Concept 138875005 Clinical finding 404684003 Finding of general physiological development 271616002 Disorder of stature 237834000 Short stature disorder 237836003 Osteogenesis imperfecta type 5 1003379004 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Developmental disorder 5294002 Developmental hereditary disorder 363070008 Osteogenesis imperfecta type 5 1003379004 SNOMED CT Concept 138875005 Clinical finding 404684003 Musculoskeletal finding 106028002 Disorder of musculoskeletal system 928000 Hereditary disorder of musculoskeletal system 363212003 Osteogenesis imperfecta type 5 1003379004 SNOMED CT Concept 138875005 Clinical finding 404684003 Functional finding 118228005 Abnormal bone formation 36123008 Osteogenesis imperfecta 78314001 Osteogenesis imperfecta type 5 1003379004 |
| ancestors | sorted most to least specific
|
| cpt crosswalks | |
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