Search Ontology: 
        
        Human Disease
            osteogenesis imperfecta type 3
- Term ID
- DOID:0110339
- Synonyms
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        - OI3
- osteogenesis imperfecta type III
- progressively deforming osteogenesis imperfecta with normal sclera
 
- Definition
- An osteogenesis imperfecta that is characterized by progressive limb and spinal deformity and normal sclerae and has_material_basis_in mutations in the COL1A1 gene on chromosome 17q21.33 or the COL1A2 gene on chromosome 7q21.3. (2)
- References
- 
    
        
        
    
    - GARD:8695
- ICD10CM:Q78.0
- MIM:259420
 
- Ontology
- Human Disease ( DOID:0110339 )
                
                    
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