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m (→Autosomal recessive polycystic kidney disease: +gross images links) |
m (→General) |
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===General=== | ===General=== | ||
*Uncommon. | *Uncommon. | ||
*Homogenous for mutated ''PKHD1 gene'' (polycystic kidney and hepatic disease).<ref name=omim263200>{{OMIM|263200}}</ref> | *Homogenous for mutated ''PKHD1 gene'' (polycystic kidney and hepatic disease).<ref name=omim263200>{{OMIM|263200}}</ref> | ||
**The same gene is implicated in [[Caroli disease]]. | |||
*Associated with congenital hepatic fibrosis | *Associated with congenital hepatic fibrosis | ||
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