. _:vb50940840 . "A familial nephrotic syndrome characterized by steroid resistance and childhood onset of proteinuria, hypoalbuminemia, hyperlipidemia, and edema that has_material_basis_in homozygous or compound heterozygous mutation in the NPHS2 gene encoding podocin on chromosome 1q25-q31."^^ . "nephrotic syndrome type 2"^^ . "OMIM:600995"^^ . . . _:vb50940840 . "disease_ontology"^^ . _:vb50940840 . "DOID:0080379"^^ . "steroid-resistant autosomal recessive nephrotic syndrome"@en . _:vb50940840 . . _:vb50940840 .