nephrotic syndrome type 12 (DOID:0080387)
Alliance: disease page
Alt IDs: OMIM:616892
Definition: A familial nephrotic syndrome characterized by early childhood onset of steroid-resistant progressive renal failure with focal segmental glomerulosclerosis that has_material_basis_in homozygous or compound heterozygous mutation in the NUP93 gene on chromosome 16q13.