Search Ontology:
Human Disease
osteogenesis imperfecta type 9
- Term ID
- DOID:0110349
- Synonyms
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- OI9
- osteogenesis imperfecta type IX
- Definition
- An osteogenesis imperfecta that has_material_basis_in mutation in the PPIB gene on chromosome 15q22. https://www.ncbi.nlm.nih.gov/pubmed/19781681
- References
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- GARD:10619
- ICD10CM:Q78.0
- MIM:259440
- Ontology
- Human Disease ( DOID:0110349 )
- is a type of
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