Disease association ontology term - MONDO:0012592 - osteogenesis imperfecta type 11
Term summary
- ID
- MONDO:0012592
- Name
- osteogenesis imperfecta type 11
- Ontology or CV name
- Disease association
- Definition
- Any osteogenesis imperfecta in which the cause of the disease is a mutation in the FKBP10 gene.
