Osteogenesis imperfecta, type IV B

disorder

SNOMED 279309008CUI C1281062

Overview

Source: MedlinePlus.gov, National Library of Medicine. Not a substitute for medical advice.

Related Conditions

Osteogenesis imperfecta type IV(parent)

Dentinogenesis imperfecta(parent)

Hereditary disorder of musculoskeletal system(parent)

Quick Facts

SNOMED CT: 279309008
UMLS CUI: C1281062
Fully Specified Name: Osteogenesis imperfecta, type IV B (disorder)
Specialists: 0
Diagnostic Biomarkers: 0

Medical Disclaimer

This information is for educational purposes only and does not constitute medical advice, diagnosis, or treatment. Always consult with a qualified healthcare provider regarding any medical condition or treatment plan.

Clinical content is derived from the SNOMED CT clinical ontology and curated medical knowledge graphs.