Fanconi renotubular syndrome 3 (DOID:0080759)
Alliance: disease page
Alt IDs: OMIM:615605
Definition: 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.