Term Name: osteogenesis imperfecta type 11
Synonyms: OI11, osteogenesis imperfecta type XI
Definition: An osteogenesis imperfecta that has_material_basis_in mutation in the FKBP10 gene on chromosome 17q21.
Ontology: Human Disease [DOID:0110351]   ( DOID:0110351 )

Relationships
is a type of: autosomal recessive disease osteogenesis imperfecta