"A familial nephrotic syndrome characterized by early childhood onset that has_material_basis_in homozygous or compound heterozygous mutation in the EMP2 gene on chromosome 16p13."^^ . _:vb50940854 . _:vb50940854 . "disease_ontology"^^ . "DOID:0080386"^^ . _:vb50940854 . . "nephrotic syndrome type 10"^^ . . "OMIM:615861"^^ . . _:vb50940854 . . _:vb50940854 .