Q78.0
Osteogenesis imperfecta
Billable FY2026 2025-10-01 → 2026-09-30
Exclusions 1 never code together
Instructional notes 2
Q78.0code
Inclusion terms
- Fragilitas ossium
- Osteopsathyrosis
Index entries leading here 17
- Syndrome — see also Disease
- Adair-Dighton syndrome (brittle bones and blue sclera, deafness) Q78.0
- Blue
- Fragile, fragility
- bone, congenital (with blue sclera) Q78.0
- Brittle
- bones disease Q78.0
- Deafness (acquired) (complete) (hereditary) (partial) H91.9
- Disease, diseased — see also Syndrome
- Eddowes (-Spurway) syndrome Q78.0
- Ekman's syndrome (brittle bones and blue sclera) Q78.0
- Osteitis — see also Osteomyelitis
- fragilitans Q78.0
- Fragilitas
- ossium (with blue sclerae) (hereditary) Q78.0
- Lobstein (-Ekman) disease or syndrome Q78.0
- Osteogenesis imperfecta Q78.0
- Osteopsathyrosis (idiopathica) Q78.0
- Spurway's syndrome Q78.0
- Van der Hoeve (-de Kleyn) syndrome Q78.0
- Vrolik's disease Q78.0
Alongside this code 8 same parent — Q78
Medications 1
MED-RT files conditions by MeSH, which carves the world differently from ICD-10. These are name matches on this code's description, offered as candidates — not as an assertion that they are this code.
Additional references
AHA Coding Clinic® Licence required
Official coding advice for this code. Published by the American Hospital Association. Not included in this installation.