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Nephrotic Syndrome Type 19

Disease ID: disease_node_19072

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DbxrefMIM:618178
SubclassofDOID_2590, DOID_0050737
Data SourceDOID
Doid Labelnephrotic syndrome type 19
Doid DescriptionA familial nephrotic syndrome that has_material_basis_in compound heterozygous mutation in the NUP160 gene on chromosome 11p11.
Has Material Basis InGENO_0000148
Disease Node Iddisease_node_19072
Doid IdDOID_0080394
LabelNephrotic Syndrome Type 19