Ehlers-Danlos and osteogenesis imperfecta syndrome
Dentinogenesis imperfecta
Neonatal lethal osteogenesis imperfecta congenita
Osteogenesis imperfecta type III
van de Hoeve syndrome
Osteogenesis imperfecta, neonatal lethal
Osteogenesis imperfecta with opalescent teeth
Osteogenesis imperfecta, retinopathy, seizures, intellectual disability syndrome
Familial doughnut lesions of skull
Osteogenesis imperfecta with blue sclerae AND normal teeth
Osteogenesis imperfecta type 5
Congenital abnormality of sclera
brittle bone syndrome
Lethal osteogenesis imperfecta
Al Gazali Nair syndrome
Fragilitas Ossium
Porak-Durante syndrome
Hereditary opalescent dentin
High bone mass osteogenesis imperfecta
Osteogenesis imperfecta type IIB
Osteogenesis imperfecta type II, dominant form
Osteogenesis imperfecta type IB
Osteogenesis imperfecta type IV with dentinogenesis imperfecta
Progressive arterial occlusive disease, hypertension, heart defect, bone fragility, brachysyndactyly syndrome
Osteogenesis imperfecta, Vrolik type
OI - Osteogenesis imperfecta
Osteogenesis imperfecta type IA
Lethal osteogenesis imperfecta with thin long bones and thin and beaded ribs
Osteoporosis with pseudoglioma
Osteogenesis imperfecta type V
Blue sclera
Osteogenesis imperfecta type IIC
brittle bone disease
Osteogenesis imperfecta with blue sclerae AND dentinogenesis imperfecta
Osteogenesis imperfecta type I
Grange syndrome
Osteogenesis imperfecta, type IV A
Osteogenesis imperfecta type II
Hereditary dysplasia of blood vessel
Osteogenesis imperfecta, recessive perinatal lethal
Calvarial doughnut lesion with bone fragility syndrome
Osteogenesis imperfecta type IIA
Grange occlusive arterial syndrome
Osteogenesis imperfecta type IV
Osteogenesis imperfecta, type IV
Osteogenesis imperfecta congenita neonatal lethal form
Abnormal blue sclerae
Vrolik disease
Osteogenesis imperfecta (disorder)
Ossiums, Fragilitas
Osteogenesis imperfecta, recessive perinatal lethal, with microcephaly AND cataracts
Doughnut lesion of calvaria and bone fragility syndrome
Osteogenesis imperfecta with normal sclerae, dominant form
Osteogenesis imperfecta, dominant perinatal lethal
Osteogenesis imperfecta type IV with normal teeth
Osteopsathyrosis
Osteogenesis imperfecta, type II
Osteogenesis imperfecta, type IV B
Osteogenesis imperfecta, type II, recessive form
Osteogenesis imperfecta, perinatal lethal
Congenital anomaly of sclera

Frequently Asked Questions

What is the ICD-10 code for osteogenesis imperfecta?

The ICD-10-CM code for osteogenesis imperfecta is Q78.0. The full clinical description is "Osteogenesis imperfecta". Q78.0 is a billable/specific code that can be used on insurance claims and medical billing.

What does ICD-10 code Q78.0 mean?

ICD-10-CM code Q78.0 represents “Osteogenesis imperfecta”. It is classified under Chapter 17: Congenital Malformations, Deformations and Chromosomal Abnormalities and 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.

How does Q78.0 relate to ICF functioning codes?

ICF (International Classification of Functioning, Disability and Health) codes describe how conditions like osteogenesis imperfecta affect a person's functioning — body functions, activities, participation, and environmental factors. AutoICD provides ICF Core Sets for 12+ conditions and can map clinical text to ICF categories automatically. Browse the ICF directory to explore functioning codes.

What is the ICD-11 equivalent of Q78.0?

Q78.0 maps to the ICD-11 code: LD24.K0 (Osteogenesis imperfecta).

Automate ICD-10 Coding With AI

Send clinical text to the AutoICD API and get back structured ICD-10 codes with confidence scores. Integrates into any EHR or billing system in minutes.

Try Free View API Docs

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.