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Cataract 41

MONDO:0007287

Any early-onset non-syndromic cataract in which the cause of the disease is a mutation in the WFS1 gene.

Also known as: CTRCT41, WFS1 early-onset non-syndromic cataract, cataract 41, cataract type 41, early-onset non-syndromic cataract caused by mutation in WFS1, cataract 41, congenital nuclear type

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

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Broader categories

Disease (618) Cataract (235) Hereditary disease (172) Eye disorder (97) Human disease (14) Lens disorder (10) Disorder of orbital region (3) Disease of genetic or genomic mechanism (2) Disorder of visual system (1) Early-onset non-syndromic cataract (1)
Trials to join now! 7 Not yet finished but already full! 1 Completed 1 Terminated 1
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