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Nephrotic Syndrome Type 10

Disease ID: disease_node_19080

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DbxrefMIM:615861
SubclassofDOID_2590, DOID_0050737
Data SourceDOID
Doid Labelnephrotic syndrome type 10
Doid DescriptionA familial nephrotic syndrome characterized by early childhood onset that has_material_basis_in homozygous or compound heterozygous mutation in the EMP2 gene on chromosome 16p13.
Has Material Basis InGENO_0000148
Disease Node Iddisease_node_19080
Doid IdDOID_0080386
LabelNephrotic Syndrome Type 10