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Nephrotic Syndrome Type 16

Disease ID: disease_node_19088

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DbxrefMIM:617783
SubclassofDOID_2590, DOID_0050737
Data SourceDOID
Doid Labelnephrotic syndrome type 16
Doid DescriptionA familial nephrotic syndrome that has_material_basis_in homozygous or compound heterozygous mutation in the KANK2 gene on chromosome 19p13.
Has Material Basis InGENO_0000148
Disease Node Iddisease_node_19088
Doid IdDOID_0080272
LabelNephrotic Syndrome Type 16