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Osteogenesis Imperfecta - Medical Condition Information

Osteogenesis Imperfecta

Brittle Bone DiseaseEkman-Lobstein Disease
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📋Overview

Osteogenesis Imperfecta (OI) is a genetic disorder characterized by fragile bones that break easily. It is caused primarily by mutations affecting type I collagen, a key protein in bone strength. OI is classified into several types based on severity and clinical features. The term 'Osteogenesis Imperfecta' is the modern and widely accepted name for this condition.

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This content is provided for general health education and awareness and is based on publicly available medical information. It is not intended to replace professional medical advice, diagnosis, or treatment, and should not be used to make healthcare decisions. Always seek the guidance of a qualified healthcare professional regarding any medical condition, medication, supplement, or procedure.

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Medical codes (for reference)

UMLS CUI: C0029434
ICD-10-CM
Q78.0
MeSH
D010013
SNOMED CT (US)
78314001

Codes are provided for reference and interoperability. They are not a diagnosis.

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