Q78.8
Other specified osteochondrodysplasias
Billable FY2026 2025-10-01 → 2026-09-30
Exclusions 1 never code together
Instructional notes 1
Q78.8code
Inclusion terms
- Osteopoikilosis
Index entries leading here 14
- Abnormal, abnormality, abnormalities — see also Anomaly
- synchondrosis Q78.8
- Synchondrosis
- abnormal (congenital) Q78.8
- Segmentation, incomplete (congenital) — see also Fusion
- bone NEC Q78.8
- Caffey's syndrome Q78.8
- Hypoplasia, hypoplastic
- cartilage hair Q78.8
- Chondrodysplasia Q78.9
- metaphyseal (Jansen's) (McKusick's) (Schmid's) Q78.8
- Dysplasia — see also Anomaly
- craniometaphyseal Q78.8
- Deficiency, deficient
- short stature homeobox gene (SHOX)
- with
- dyschondrosteosis Q78.8
- with
- short stature homeobox gene (SHOX)
- Leri's pleonosteosis Q78.8
- Osteochondrodysplasia Q78.9
- specified NEC Q78.8
- Osteopathia condensans disseminata Q78.8
- Osteopoikilosis Q78.8
- Stippled epiphyses Q78.8
- Synostosis (congenital) Q78.8
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.