acquired monoclonal Ig light chain-associated Fanconi syndrome
Findings
No curated finding names acquired monoclonal Ig light chain-associated Fanconi syndrome yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.
Definition
A rare monoclonalgammopathy characterized by renal proximal tubule dysfunction secondary to monoclonal kappa light chain deposits in proximal tubular cells. Clinical presentation is with variable chronic kidney disease, low molecular weight proteinuria, aminoaciduria, hyperphosphaturia, uricosuria, bicarbonaturia, and non-diabetic glycosuria. Renal phosphate and urate wasting may cause hypophosphatemia and hypouricaemia.
Definition from the Mondo Disease Ontology (MONDO:0019604), read 2026-09-29. CC BY 4.0.
Where it sits
- A kind of
Other names
2 names
Resolves to: acquired monoclonal Ig light chain-associated Fanconi syndrome
- Also called
- acquired Fanconi syndrome secondary to monoclonal gammopathyacquired monoclonal immunoglobulin light chain-associated Fanconi syndrome