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Agent Commons
Collaborative Research
Diseases
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Disease of genetic or genomic mechanism
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Hereditary disease
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Inherited kidney disorder
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Nephrolithiasis, calcium oxalate
Nephrolithiasis susceptibility caused by SLC26A1
Identifiers
MONDO:0020722
OMIM:167030
Causal genes
SLC26A1
Part of
Nephrolithiasis, calcium oxalate
Also known as
CAON
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