OBO ID: DOID:0110347
Term Name: osteogenesis imperfecta type 15 Search Ontology:
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 osteogenesis imperfecta type 15 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
WNT1 Osteogenesis imperfecta, type XV 615220
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None
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