Monarch Disease Ontology id MONDO_0014752 (nephrotic syndrome, type 11) is any familial nephrotic syndrome in which the cause of the disease is a mutation in the NUP107 gene. Also known as: NPHS11, NUP107 familial nephrotic syndrome, Nup107 familial nephrotic syndrome, familial nephrotic syndrome caused by mutation in NUP107, familial nephrotic syndrome caused by mutation in Nup107, nephrotic syndrome, type 11; NPHS11.