Search Ontology:
Human Disease
osteogenesis imperfecta type 11
- Term ID
- DOID:0110351
- Synonyms
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- OI11
- osteogenesis imperfecta type XI
- Definition
- An osteogenesis imperfecta that has_material_basis_in mutation in the FKBP10 gene on chromosome 17q21. https://www.ncbi.nlm.nih.gov/pubmed/20362275
- References
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- ICD10CM:Q78.0
- MIM:610968
- Ontology
- Human Disease ( DOID:0110351 )
- is a type of
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Zebrafish Models