|
DOID:0110351 - osteogenesis imperfecta type 11
Disease Ontology Definition:An osteogenesis imperfecta that has_material_basis_in mutation in the FKBP10 gene on chromosome 17q21.
Synonyms: OI11, osteogenesis imperfecta type XI,
Echinobase Genes :
MIM:610968 - osteogenesis imperfecta, type xi; oi11 |
Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s):
osteogenesis imperfecta (is_a)