Monarch Disease Ontology id MONDO_0014817 (nephrotic syndrome, type 12) is any familial nephrotic syndrome in which the cause of the disease is a mutation in the NUP93 gene. Also known as: NPHS12, NUP93 familial nephrotic syndrome, familial nephrotic syndrome caused by mutation in NUP93, nephrotic syndrome, type 12; NPHS12.