Search Ontology:
Human Disease
osteogenesis imperfecta type 5
- Term ID
- DOID:0110344
- Synonyms
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- OI5
- osteogenesis imperfecta type V
- Definition
- An osteogenesis imperfecta that has_material_basis_in mutation in the IFITM5 gene on chromosome 11p15. https://www.ncbi.nlm.nih.gov/pubmed/22863190
- References
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- GARD:8699
- ICD10CM:Q78.0
- MIM:610967
- Ontology
- Human Disease ( DOID:0110344 )
- is a type of
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Zebrafish Models