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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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Familial juvenile hyperuricemic nephropathy
Tubulointerstitial kidney disease, autosomal dominant 6
Identifiers
MONDO:0976234
OMIM:621106
Causal genes
APOA4
Part of
Familial juvenile hyperuricemic nephropathy
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