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Nephrotic Syndrome Type 6

Disease ID: disease_node_19082

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DbxrefMIM:614196
SubclassofDOID_2590, DOID_0050737
Data SourceDOID
Doid Labelnephrotic syndrome type 6
Doid DescriptionA familial nephrotic syndrome that has_material_basis_in homozygous mutation in the PTPRO gene on chromosome 12p12.
Has Material Basis InGENO_0000148
Disease Node Iddisease_node_19082
Doid IdDOID_0080384
LabelNephrotic Syndrome Type 6