_:vb50941577 . . _:vb50941577 . "A Fanconi syndrome that is characterized by characterized by rickets, impaired growth, glucosuria, generalized aminoaciduria, phosphaturia, metabolic acidosis, and low molecular weight proteinuria and that has_material_basis_in heterozygous mutation in the EHHADH gene on chromosome 3q27."^^ . _:vb50941577 . "disease_ontology"^^ . "DOID:0080759"^^ . . _:vb50941577 . _:vb50941577 . . . "Fanconi renotubular syndrome 3"@en . "OMIM:615605"^^ .