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Nephrotic Syndrome Type 18

Disease ID: disease_node_19073

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DbxrefMIM:618177
SubclassofDOID_2590, DOID_0050737
Data SourceDOID
Doid Labelnephrotic syndrome type 18
Doid DescriptionA familial nephrotic syndrome that has_material_basis_in by homozygous or compound heterozygous mutation in the NUP133 gene on chromosome 1q42.
Has Material Basis InGENO_0000148
Disease Node Iddisease_node_19073
Doid IdDOID_0080393
LabelNephrotic Syndrome Type 18