Search Ontology:
Human Disease

osteogenesis imperfecta type 7

Term ID
DOID:0110337
Synonyms
  • OI7
  • osteogenesis imperfecta type VII
Definition
An osteogenesis imperfecta that has_material_basis_in mutation in the CRTAP gene on chromosome 3p22. https://www.ncbi.nlm.nih.gov/pubmed/17055431
References
Ontology
Human Disease   ( DOID:0110337 )
Relationships
is a type of
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
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