OBO ID: DOID:0110351
Term Name: osteogenesis imperfecta type 11 Search Ontology:
Synonyms:
  • OI11
  • osteogenesis imperfecta type XI
Definition: An osteogenesis imperfecta that has_material_basis_in mutation in the FKBP10 gene on chromosome 17q21. https://www.ncbi.nlm.nih.gov/pubmed/20362275
References:
Ontology: Human Disease   ( DOID:0110351 )
Relationships
is a type of:
OTHER osteogenesis imperfecta type 11 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
FKBP10 Osteogenesis imperfecta, type XI 610968
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None
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