Search Ontology:
Human Disease

osteogenesis imperfecta type 15

Term ID
DOID:0110347
Synonyms
  • OI15
  • osteogenesis imperfecta type XV
Definition
An osteogenesis imperfecta that has_material_basis_in mutation in the WNT1 gene on chromosome 12q13. https://www.ncbi.nlm.nih.gov/pubmed/23499309
References
Ontology
Human Disease   ( DOID:0110347 )
Relationships
is a type of
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
Citations
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