Primary Fanconi syndrome

MONDO:0007600

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.

Also known as: FRTS1, Fanconi renotubular syndrome 1, primary Fanconi renotubular syndrome

1 clinical trial for this condition and its sub-types, 0 tagged with Primary Fanconi syndrome itself.

Follow this condition to get notified about new trials

Where it sits in the disease tree

Browse by category →

Part of

↑ Inherited Fanconi renotubular syndrome (0)

Sub-types of Primary Fanconi syndrome

Including sub-types (1) Tagged with Primary Fanconi syndrome (0)

We haven't found any trials for this condition yet. Follow it to get notified when new trials appear.