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
Ontology
Human Disease   ( DOID:0110350 )
Relationships
is a type of
Other Pages
Genes Involved
Zebrafish Models