Laboratory for Molecular Diagnostics

Center for Nephrology and Metabolic Disorders

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Hereditary FSGS type 3

Hereditary FSGS type 3 is an autosomal dominant disorder caused by mutations of the CD2AP 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
		CD2AP
	Hereditary FSGS type 4
	Hereditary FSGS type 5
	Hereditary FSGS type 6
	Hereditary FSGS type 7
	Norum disease

References:

1.	Büscher AK et al. (2012) Mutations in podocyte genes are a rare cause of primary FSGS associated with ESRD in adult patients. [^]

2.	Kim JM et al. (2003) CD2-associated protein haploinsufficiency is linked to glomerular disease susceptibility. [^]