Osteogenesis imperfecta with blue sclerae AND dentinogenesis imperfecta

disorder

SNOMED 63890001CUI C5574661

Overview

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

Related Conditions

Dentinogenesis imperfecta(parent)

Hereditary disorder of the visual system(parent)

Osteogenesis imperfecta type I(parent)

Congenital anomaly of sclera(parent)

Lesion of sclera(parent)

Quick Facts

SNOMED CT: 63890001
UMLS CUI: C5574661
Fully Specified Name: Osteogenesis imperfecta with blue sclerae AND dentinogenesis imperfecta (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.