OBO ID: DOID:0110345
Term Name: osteogenesis imperfecta type 16 Search Ontology:
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 osteogenesis imperfecta type 16 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
CREB3L1 Osteogenesis imperfecta, type XVI 616229
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None
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