Search Ontology:
Human Disease

osteogenesis imperfecta type 16

Term ID
DOID:0110345
Synonyms
  • chromosome 11p11.2 deletion syndrome 91.3-KB
  • OI16
  • osteogenesis imperfecta type XVI
Definition
An osteogenesis imperfecta that has_material_basis_in contiguous gene deletion on chromosome 11p11. https://www.ncbi.nlm.nih.gov/pubmed/24079343
References
Ontology
Human Disease   ( DOID:0110345 )
Relationships
is a type of
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
Citations
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