Search Ontology:
Human Disease
osteogenesis imperfecta type 6
- Term ID
- DOID:0110350
- Synonyms
-
- OI6
- osteogenesis imperfecta type VI
- Definition
- An osteogenesis imperfecta that has_material_basis_in mutation in the SERPINF1 gene on chromosome 17p13.3. https://www.ncbi.nlm.nih.gov/pubmed/21353196
- References
-
- GARD:8700
- ICD10CM:Q78.0
- MIM:613982
- Ontology
- Human Disease ( DOID:0110350 )
- is a type of
-
Other Pages
Genes Involved
Zebrafish Models
Citations