"A familial nephrotic syndrome characterized by neonatal or early childhood onset steroid resistant renal disease that has_material_basis_in homozygous or compound heterozygous mutation in the ARHGDIA gene on chromosome 17q25."^^ . . . "OMIM:615244"^^ . "nephrotic syndrome type 8"^^ . _:vb50940860 . . _:vb50940860 . _:vb50940860 . . "disease_ontology"^^ . "DOID:0080389"^^ . _:vb50940860 . _:vb50940860 .