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Osteogenesis Imperfecta Type 6

Disease ID: disease_node_15618

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DbxrefGARD:8700, ICD10CM:Q78.0, MIM:613982
SubclassofDOID_12347, DOID_0050177
Data SourceDOID
SynonymsOI6, osteogenesis imperfecta type VI
Doid Labelosteogenesis imperfecta type 6
Doid DescriptionAn osteogenesis imperfecta that has_material_basis_in mutation in the SERPINF1 gene on chromosome 17p13.3.
Disease Node Iddisease_node_15618
Doid IdDOID_0110350
Disease Has Basis InSO_0000704
LabelOsteogenesis Imperfecta Type 6