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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

Focal, segmental glomerulosclerosis (FSGS)
ALG13
ARHGAP24
CLU
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
ITGA9
LAMA5
NXF5

References:

1.

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

external link
2.

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

external link
3.

OMIM.ORG article

Omim 607832 external link
Update: Aug. 14, 2020
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