Laboratory for Molecular Diagnostics
Center for Nephrology and Metabolic Disorders

Hyperoxaluria type 3

The autosomal recessive oxalosis 3 is hyperoxaluria, oxalate nephrolithiasis and nephrocalcinosis due to mutations of the HOGA1 gene.

Systematic

Hyperoxaluria
Hyperoxaluria type 1
Hyperoxaluria type 2
Hyperoxaluria type 3
HOGA1

References:

1.

Belostotsky R et al. (2010) Mutations in DHDPSL are responsible for primary hyperoxaluria type III.

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2.

OMIM.ORG article

Omim 613616 [^]
Update: April 29, 2019