Fanconi-Like Syndrome, also known as fanconi like syndrome, is related to fanconi syndrome and congenital intrinsic factor deficiency. An important gene associated with Fanconi-Like Syndrome is SLC6A18 (Solute Carrier Family 6 Member 18), and among its related pathways/superpathways are Transport of inorganic cations/anions and amino acids/oligopeptides and Nuclear receptors meta-pathway. Affiliated tissues include lung and kidney, and related phenotypes are recurrent lower respiratory tract infections and osteomyelitis