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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

11 clinical trials for this condition and its sub-types.

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Broader categories

Disease (618) Kidney disorder (202) Hereditary disease (172) Urinary system disorder (62) Human disease (14) Autosomal recessive disease (4) Nephronophthisis (4) Disease of genetic or genomic mechanism (2) Renal tubule disorder (1) Autosomal genetic disease (0)
Trials to join now! 5 Not yet recruiting 2 Not yet finished but already full! 3 Completed 1
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