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Osteogenesis Imperfecta Type 17

Disease ID: disease_node_15630

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DbxrefICD10CM:Q78.0, MIM:616507
SubclassofDOID_12347, DOID_0050737
Data SourceDOID
SynonymsOI17, osteogenesis imperfecta type XVII
Doid Labelosteogenesis imperfecta type 17
Doid DescriptionAn osteogenesis imperfecta that has_material_basis_in mutation in the SPARC gene on chromosome 5q33.
Has Material Basis InGENO_0000148
Disease Node Iddisease_node_15630
Doid IdDOID_0110338
LabelOsteogenesis Imperfecta Type 17