Disease-gene associations mined from literature

Human genes for nephrotic syndrome type 7

Nephrotic syndrome type 7 [DOID:0080388]

A familial nephrotic syndrome characterized by onset in the first decade of life of progressive renal disease with proteinuria and membranoproliferative glomerulonephritis that has_material_basis_in homozygous or compound heterozygous mutation in the DGKE gene on chromosome 17q22.

Synonyms:  nephrotic syndrome type 7,  DOID:0080388,  Ig-mediated MPGN,  Ig-mediated membranoproliferative glomerulonephritis,  Immunoglobulin-mediated MPGN ...