Term Name: osteogenesis imperfecta type 10
Synonyms: OI10, osteogenesis imperfecta type X
Definition: An osteogenesis imperfecta that has_material_basis_in mutation in the SERPINH gene on chromosome 11q13.
Ontology: Human Disease [DOID:0110346]   ( DOID:0110346 )

Relationships
is a type of: autosomal recessive disease osteogenesis imperfecta