Laboratory for Molecular Diagnostics
Center for Nephrology and Metabolic Disorders
Moldiag Diseases Genes Support Contact

Hereditary FSGS type 9

Hereditary FSGS type 9 is an autosomal rezcessive disorder caused by mutations of the CRB2 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
Hereditary FSGS type 6
Hereditary FSGS type 7
Hereditary FSGS type 8
Hereditary FSGS type 9
CRB2
ITGA9
LAMA5
NXF5

References:

1.

Ebarasi L et al. (2015) Defects of CRB2 cause steroid-resistant nephrotic syndrome.

external link
Update: Nov. 3, 2022
Copyright © 2005-2024 by Center for Nephrology and Metabolic Disorders, Dr. Mato Nagel, MD
Albert-Schweitzer-Ring 32, D-02943 Weißwasser, Germany, Tel.: +49-3576-287922, Fax: +49-3576-287944
Sitemap | Webmail | Disclaimer | Privacy Issues | Website Credits