LD24.K0
Osteogenesis imperfecta
Osteogenesis imperfecta
Classification
ICD-11
Chapter
20: Developmental AnomaliesBlock
LD20-LD2ZParent Code
LD24.KICD-10 Mapping
1 equivalentWHO Foundation
View on WHOICD-10 Equivalents(1)
ICD-10 Equivalents
View full mappingCorresponding ICD-10-CM codes from the WHO crosswalk mapping
Also Known As / Clinical Terms(10)
SNOMED CT ↗
- Congenital abnormality of sclera32809005
- Brittle bone disease78314001
- Dentinogenesis imperfecta196286005
- Abnormal blue sclerae204164000
- Hereditary dysplasia of blood vessel461415008
- Grange occlusive arterial syndrome717824007
- Calvarial doughnut lesion with bone fragility syndrome720598005
- Al Gazali Nair syndrome722110003
- Ehlers-Danlos and osteogenesis imperfecta syndrome733457006
- High bone mass osteogenesis imperfecta782781006
Frequently Asked Questions
What is the ICD-11 code for osteogenesis imperfecta?
The ICD-11 code for osteogenesis imperfecta is LD24.K0. The full clinical description is "Osteogenesis imperfecta".
What does ICD-11 code LD24.K0 mean?
ICD-11 code LD24.K0 represents “Osteogenesis imperfecta”. It is classified under Chapter 20: Developmental Anomalies.
What chapter is LD24.K0 in?
LD24.K0 is in Chapter 20: Developmental Anomalies (codes LA00-LD9Z).
What is the ICD-10 equivalent of ICD-11 code LD24.K0?
LD24.K0 maps to the ICD-10 code: Q78.0 (Osteogenesis imperfecta). This is an equivalent mapping.
What is the difference between ICD-10 and ICD-11?
ICD-11 is the latest revision of the WHO's International Classification of Diseases, succeeding ICD-10. Key differences include: a fully digital-first design, new chapters for sleep-wake disorders, sexual health, and traditional medicine, improved coding for rare diseases, and better integration with electronic health records through extension codes.
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Includes SNOMED Clinical Terms® (SNOMED CT®) used by permission of SNOMED International. Includes content from the UMLS Metathesaurus, courtesy of the U.S. National Library of Medicine.