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
-
- GARD:8701
- ICD10CM:Q78.0
- MESH:C565200
- MIM:610682
- Ontology
- Human Disease ( DOID:0110337 )
- is a type of
-
Other Pages
Genes Involved
Zebrafish Models