Laboratory for Molecular Diagnostics
Center for Nephrology and Metabolic Disorders

Hereditary FSGS type 5

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

Systematic

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

References:

1.

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

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2.

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

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3.

OMIM.ORG article

Omim 613237 [^]
Update: April 29, 2019