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DOID:0110345 - osteogenesis imperfecta type 16
Disease Ontology Definition:An osteogenesis imperfecta that has_material_basis_in contiguous gene deletion on chromosome 11p11.
Synonyms: OI16, chromosome 11p11.2 deletion syndrome 91.3-KB, osteogenesis imperfecta type XVI,
Echinobase Genes :
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)