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 membranoproliferative glomerulonephritis, Ig-mediated MPGN, immunoglobulin-mediated membranoproliferative glomerulonephritis ...