primary Fanconi syndrome https://github.com/monarch-initiative/mondo/issues/3113 https://rarediseases.info.nih.gov/diseases/9118/primary-fanconi-syndrome https://www.malacards.org/card/primary_fanconi_renotubular_syndrome UMLS:C1857395 Orphanet:3337 Fanconi renotubular syndrome 1 FRTS1 GARD:0009118 MONDO:0007600 MEDGEN:341765 NCIT:C123229 primary Fanconi renotubular syndrome A condition in which the kidneys do not absorb certain substances into the body. These substances, such as cysteine, fructose, galactose, or glycogen, are lost in the urine. Fanconi syndrome is thought to be caused by genetic and environmental factors, and it may be diagnosed at any age. Symptoms of Fanconi syndrome include increased urine production (which may cause dehydration), weakness, and abnormalities of the bones. inherited Fanconi renotubular syndrome