Term Name:	osteogenesis imperfecta type 16
Synonyms:	chromosome 11p11.2 deletion syndrome 91.3-KB, OI16, osteogenesis imperfecta type XVI
Definition:	An osteogenesis imperfecta that has_material_basis_in contiguous gene deletion on chromosome 11p11.
Ontology:	Human Disease [DOID:0110345]   ( DOID:0110345 )