Nephronophthisis 13

MONDO:0013718

A nephronophthisis that has material basis in homozygous or compound heterozygous mutation in the WDR19 gene on chromosome 4p14.

Also known as: NPHP13, nephronophthisis 13, nephronophthisis type 13

1 clinical trial for this condition and its sub-types, 0 tagged with Nephronophthisis 13 itself.

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