OBO ID: DOID:0110344
Term Name: osteogenesis imperfecta type 5 Search Ontology:
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 osteogenesis imperfecta type 5 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
IFITM5 Osteogenesis imperfecta, type V 610967
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None
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