Osteogenesis imperfecta, type IV B 279309008

SNOMED CT code

SNOMED code

279309008

name

Osteogenesis imperfecta, type IV B

status

active

date introduced

2002-01-31

fully specified name(s)

Osteogenesis imperfecta, type IV B (disorder)

synonyms

Osteogenesis imperfecta, type IV B
Osteogenesis imperfecta type IV with dentinogenesis imperfecta

attributes - group1

Pathological process

Pathological developmental process 308490002

Occurrence

Congenital 255399007

Associated morphology

Dysplasia 25723000

Finding site

Bone structure 272673000

attributes - group2

Has interpretation

Abnormal 263654008

Interprets

Bone formation 83323007

attributes - group3

Occurrence

Congenital 255399007

Finding site

Dentin structure 84540008

Associated morphology

Morphologically abnormal structure 49755003

Pathological process

Pathological developmental process 308490002

parents

Dentinogenesis imperfecta 196286005
Osteogenesis imperfecta with normal sclerae, dominant form 205497004
Hereditary disorder of musculoskeletal system 363212003

hierarchies

a selection of possible paths

SNOMED CT Concept 138875005
Clinical finding 404684003
Disease 64572001
Developmental disorder 5294002
Developmental hereditary disorder 363070008
Dentinogenesis imperfecta 196286005
Osteogenesis imperfecta, type IV B 279309008

SNOMED CT Concept 138875005
Clinical finding 404684003
Functional finding 118228005
Abnormal bone formation 36123008
Osteogenesis imperfecta 78314001
Osteogenesis imperfecta with normal sclerae, dominant form 205497004
Osteogenesis imperfecta, type IV B 279309008

SNOMED CT Concept 138875005
Clinical finding 404684003
Musculoskeletal finding 106028002
Disorder of musculoskeletal system 928000
Hereditary disorder of musculoskeletal system 363212003
Osteogenesis imperfecta, type IV B 279309008

ancestors

sorted most to least specific

Dentinogenesis imperfecta 196286005
Osteogenesis imperfecta with normal sclerae, dominant form 205497004
Hereditary disorder of musculoskeletal system 363212003
Autosomal dominant hereditary disorder 11164009
Osteogenesis imperfecta 78314001
Hereditary disorder of tooth 1148766007
Developmental hereditary disorder 363070008
Congenital anomaly of tooth 422977003
Disorder of hard tissues of teeth 46557008
Autosomal hereditary disorder 1899006
Skeletal dysplasia 105986008
Congenital anomaly of digestive organ 128332003
Abnormal bone formation 36123008
Congenital anomaly of skeletal bone 8447006
Digestive system hereditary disorder 363080007
Congenital abnormality of oral cavity 282041002
Malformation of tooth 422775003
Congenital anomaly of jaw 95473006
Congenital anomaly of musculoskeletal system 73573004
Hereditary disorder by system 363137000
Functional finding 118228005
Disorder of bone development 371521007
Disorder of tooth development 371136004
Congenital anomaly of mouth 128334002
Hereditary disease 32895009
Tooth disorder 234947003
Disorder of bone 76069003
Congenital anomaly of head 87290003
Congenital malformation of upper alimentary tract 275262008
Genetic disease 782964007
Disorder of teeth AND/OR supporting structures 105995000
Disorder of skeletal system 88230002
Tooth finding 278544002
Disorder of digestive organ 76712006
Bone finding 118953000
Congenital anomaly of digestive tract 95470009
Oral cavity finding 116337000
Congenital anomaly of digestive system 69518005
Disorder of musculoskeletal system 928000
Disease of mouth 118938008
Disorder of jaw 37156001
Congenital malformation 276654001
Finding of mouth region 423066003
Musculoskeletal finding 106028002
Disorder of head 118934005
Disorder of upper digestive tract 50410009
Developmental disorder 5294002
Finding of head region 298364001
Congenital disease 66091009
Disorder of digestive tract 84410009
Head finding 406122000
Disorder of digestive system 53619000
Finding of head and neck region 118254002
Disorder of body system 362965005
Digestive system finding 386617003
Disease 64572001
Clinical finding 404684003
SNOMED CT Concept 138875005

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SNOMED CT Concept 138875005

Clinical finding 404684003

Disease 64572001

Developmental disorder 5294002

Developmental hereditary disorder 363070008

Dentinogenesis imperfecta 196286005

Osteogenesis imperfecta, type IV B 279309008

SNOMED CT code