fibronectin glomerulopathy - Ontology Report

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Term:	fibronectin glomerulopathy	go back to main search page
Accession:	EFO:MONDO:0007671	browse the term
Definition:	A hereditary kidney disease characterized by proteinuria, type IV renal tubular acidosis, microscopic hematuria and hypertension that may lead to end-stage renal failure in the second to sixth decade of life.
Synonyms:	exact_synonym:	GFND; glomerulopathy with fibronectin deposits
	related_synonym:	GFND1; GFND2; glomerular nephritis, familial, with fibronectin deposits; glomerulopathy with fibronectin deposits 1; glomerulopathy with fibronectin deposits 2; glomerulopathy with giant fibrillar deposits; lobular glomerulopathy, familial
	alt_id:	MONDO:0007671
	xref:	GARD:15019; MEDGEN:854773; MESH:C536826; MESH:C562900; MIM:PS137950; NANDO:2200133; ORDO:84090; SCTID:236535001; UMLS:C3888104; icd11.foundation:1877494378
	see_also:	https://rarediseases.info.nih.gov/diseases/9268/glomerulopathy-with-fibronectin-deposits-1" xsd:anyURI {source="GARD:0009268

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Term paths to the root

Path 1
Term	Annotations
experimental factor	0
material property	0
disposition	0
disease	0
genetic disorder	0
inherited kidney disorder	0
fibronectin glomerulopathy	0
glomerulopathy with fibronectin deposits 2	0
Path 2
Term	Annotations
experimental factor	0
material property	0
disposition	0
disease	0
urinary system disease	0
kidney disease	0
glomerular disease	0
fibronectin glomerulopathy	0
glomerulopathy with fibronectin deposits 2	0

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