Search Ontology:
Human Disease

osteogenesis imperfecta type 17

Term ID
DOID:0110338
Synonyms
  • OI17
  • osteogenesis imperfecta type XVII
Definition
An osteogenesis imperfecta that has_material_basis_in mutation in the SPARC gene on chromosome 5q33. https://www.ncbi.nlm.nih.gov/pubmed/26027498
References
Ontology
Human Disease   ( DOID:0110338 )
Relationships
is a type of
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
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