OBO ID: DOID:0110348
Term Name: osteogenesis imperfecta type 12 Search Ontology:
Synonyms:
  • OI12
  • osteogenesis imperfecta type XII
Definition: An osteogenesis imperfecta that has_material_basis_in mutation in the SP7 gene on chromosome 12q13. https://www.ncbi.nlm.nih.gov/pubmed/20579626
References:
Ontology: Human Disease   ( DOID:0110348 )
Relationships
is a type of:
OTHER osteogenesis imperfecta type 12 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
SP7 Osteogenesis imperfecta, type XII 613849
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None
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