Search Ontology:
Human Disease

osteogenesis imperfecta type 5

Term ID
DOID:0110344
Synonyms
  • OI5
  • osteogenesis imperfecta type V
Definition
An osteogenesis imperfecta that has_material_basis_in mutation in the IFITM5 gene on chromosome 11p15. https://www.ncbi.nlm.nih.gov/pubmed/22863190
References
Ontology
Human Disease   ( DOID:0110344 )
Relationships
is a type of
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
Citations
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