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Osteogenesis Imperfecta Type 5

Disease ID: disease_node_15624

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DbxrefGARD:8699, ICD10CM:Q78.0, MIM:610967
SubclassofDOID_0050736, DOID_12347
Data SourceDOID
SynonymsOI5, osteogenesis imperfecta type V
Doid Labelosteogenesis imperfecta type 5
Doid DescriptionAn osteogenesis imperfecta that has_material_basis_in mutation in the IFITM5 gene on chromosome 11p15.
Has Material Basis InGENO_0000147
Disease Node Iddisease_node_15624
Doid IdDOID_0110344
LabelOsteogenesis Imperfecta Type 5