nephrotic syndrome type 23 (DOID:0112266)
Alliance: disease page
Synonyms: NPHS23
Alt IDs: OMIM:619201
Definition: A familial nephrotic syndrome characterized by onset of proteinuria in the first or second decade of life, mesangial hypercellularity, focal segmental glomerulosclerosis, and effacement of podocyte foot processes that has_material_basis_in homozygous or compound heterozygous mutation in the KIRREL1 gene on chromosome 1q23.1.