Nephronophthisis 11

MONDO:0013302

A nephronophthisis that has material basis in homozygous or compound heterozygous mutation in the TMEM67 gene on chromosome 8q22.1.

Also known as: NPHP11, nephronophthisis 11, nephronophthisis type 11

1 clinical trial for this condition and its sub-types, 0 tagged with Nephronophthisis 11 itself.

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