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Fanconi renotubular syndrome
Disease Summary
Associated Targets (7)
Tbio
4
Tchem
3
Mondo Description A genetic or acquired disorder characterized by impairment of the function of the proximal tubules of the kidney. It results in decreased reabsorption of electrolytes, glucose, amino acids, and other nutrients.
Disease Ontology Description A renal tubular transport disease of the proximal renal tubes characterized by glucosuria, phosphaturia, generalized aminoaciduria and HCO3 wasting.
Counts of Target Development Levels for diseases known to be associated with this disease. If the disease has a valid DOID, targets known to be associated with all child diseases are aggregated. Click "Explore Associated Targets" to view more facets and details for the target list.
Description from Mondo Disease Ontology.
Description from Disease Ontology
DataSources which have contributed target associations to this disease, and the identifiers by which the disease is referenced.
DC:0000148
DOID:1062
GARD:0009120
MESH:D005198
NCIT:C3034
SCTID:40488004
UMLS:C0015624
MONDO:0001083
High level summary of knowledge for a disease, including descriptions and datasource references.