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glomerulopathy with fibronectin deposits 2

Disease Summary
Associated Targets (1)
Tchem

1


GARD Rare
Mondo Description Any fibronectin glomerulopathy in which the cause of the disease is a mutation in the FN1 gene.
Uniprot Description Genetically heterogeneous autosomal dominant disorder characterized clinically by proteinuria, microscopic hematuria, and hypertension that leads to end-stage renal failure in the second to fifth decade of life.
Mondo Term and Equivalent IDs
MONDO:0011165:  glomerulopathy with fibronectin deposits 2
GARD:0009914: 
SCTID:722759007: