Laboratory for Molecular Diagnostics

Center for Nephrology and Metabolic Disorders

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Hereditary FSGS type 5

Hereditary FSGS type 5 is an autosomal dominant disorder caused by mutations of the INF2 gene.

Systematic

Glomerulosclerosis
	ARHGAP24
	CLU
	Familial partial lipodystrophy type 2
	Frasier syndrome
	Glycogen storage disease 1a
	Hereditary FSGS type 1
	Hereditary FSGS type 2
	Hereditary FSGS type 3
	Hereditary FSGS type 4
	Hereditary FSGS type 5
		INF2
	Hereditary FSGS type 6
	Hereditary FSGS type 7
	Norum disease

References:

1.	Brown EJ et al. (2010) Mutations in the formin gene INF2 cause focal segmental glomerulosclerosis. [^]

2.	D'Agati VD et al. (2004) Pathologic classification of focal segmental glomerulosclerosis: a working proposal. [^]