Q78.0
BillableOsteogenesis imperfecta
Osteogenesis imperfecta
Status
Billable / Specific
Parent Code
Q78Coding Notes
Also Known As / Clinical Terms
SNOMED CT
- Neonatal lethal osteogenesis imperfecta congenita7134007
- Osteogenesis imperfecta type II, dominant form7134007
- Osteogenesis imperfecta, dominant perinatal lethal7134007
- Osteogenesis imperfecta, recessive perinatal lethal, with microcephaly AND cataracts15552004
- Congenital abnormality of sclera32809005
- Congenital anomaly of sclera32809005
- Osteogenesis imperfecta type IB63890001
- Osteogenesis imperfecta with blue sclerae AND dentinogenesis imperfecta63890001
- Osteogenesis imperfecta with opalescent teeth63890001
- Osteogenesis imperfecta type IA64404003
- Osteogenesis imperfecta with blue sclerae AND normal teeth64404003
- Brittle bone disease78314001
- Brittle bone syndrome78314001
- Fragilitas ossium78314001
- OI - Osteogenesis imperfecta78314001
- Osteogenesis imperfecta78314001
- Osteopsathyrosis78314001
- Osteogenesis imperfecta, Vrolik type86470003
- Osteogenesis imperfecta, recessive perinatal lethal86470003
- Osteogenesis imperfecta, type II, recessive form86470003
- Porak-Durante syndrome86470003
- Vrolik disease86470003
- Dentinogenesis imperfecta196286005
- Hereditary opalescent dentin196286005
- Abnormal blue sclerae204164000
- Blue sclera204164000
- Lethal osteogenesis imperfecta205496008
- Osteogenesis imperfecta type II205496008
- Osteogenesis imperfecta, perinatal lethal205496008
- Osteogenesis imperfecta, type II205496008
- Osteogenesis imperfecta type IV205497004
- Osteogenesis imperfecta with normal sclerae, dominant form205497004
- Osteogenesis imperfecta, type IV205497004
- Osteogenesis imperfecta congenita neonatal lethal form254110009
- Osteogenesis imperfecta type IIA254110009
- Osteogenesis imperfecta, neonatal lethal254110009
- Osteogenesis imperfecta type IIB254111008
- Osteoporosis with pseudoglioma254112001
- Osteogenesis imperfecta type IV with dentinogenesis imperfecta279309008
- Osteogenesis imperfecta, type IV B279309008
- Osteogenesis imperfecta type IV with normal teeth280159008
- Osteogenesis imperfecta, type IV A280159008
- Osteogenesis imperfecta type I385482004
- van de Hoeve syndrome385482004
- Osteogenesis imperfecta type III385483009
- Hereditary dysplasia of blood vessel461415008
- Grange occlusive arterial syndrome717824007
- Grange syndrome717824007
- Progressive arterial occlusive disease, hypertension, heart defect, bone fragility, brachysyndactyly syndrome717824007
- Calvarial doughnut lesion with bone fragility syndrome720598005
- Doughnut lesion of calvaria and bone fragility syndrome720598005
- Familial doughnut lesions of skull720598005
- Al Gazali Nair syndrome722110003
- Osteogenesis imperfecta, retinopathy, seizures, intellectual disability syndrome722110003
- Ehlers-Danlos and osteogenesis imperfecta syndrome733457006
- High bone mass osteogenesis imperfecta782781006
- Osteogenesis imperfecta type 51003379004
- Osteogenesis imperfecta type V1003379004
- Lethal osteogenesis imperfecta with thin long bones and thin and beaded ribs1197018005
- Osteogenesis imperfecta type IIC1197018005
UMLS
- Brittle Bone DiseaseC0029434
- Brittle bone diseaseC0029434
- Brittle bone syndromeC0029434
- Fragilitas OssiumC0029434
- Fragilitas ossiumC0029434
- OI - Osteogenesis imperfectaC0029434
- OSTEOGENESIS IMPERFECTAC0029434
- Ossiums, FragilitasC0029434
- Osteogenesis ImperfectaC0029434
- Osteogenesis imperfectaC0029434
- Osteogenesis imperfecta (disorder)C0029434
- OsteopsathyrosisC0029434
- brittle bone diseaseC0029434
- brittle bone syndromeC0029434
- osteogenesis imperfectaC0029434
Frequently Asked Questions
What is ICD-10 code Q78.0?
ICD-10-CM code Q78.0 represents "Osteogenesis imperfecta". It is a billable/specific code that can be used on a claim.
Is Q78.0 a billable code?
Yes, Q78.0 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.
What chapter is Q78.0 in?
Q78.0 is in Chapter 17: Congenital Malformations, Deformations and Chromosomal Abnormalities (codes Q00-Q99).
What SNOMED CT codes does Q78.0 map to?
Q78.0 maps to 26 SNOMED CT concepts: 204164000, 722110003, 78314001, 720598005, 32809005, and 21 more. SNOMED CT is a clinical terminology used in electronic health records.
What are the UMLS CUIs for Q78.0?
Q78.0 is linked to 1 UMLS Concept Unique Identifier: C0029434. The UMLS (Unified Medical Language System) integrates multiple biomedical vocabularies maintained by the U.S. National Library of Medicine.
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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.