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Cataract 35

MONDO:0012260

A cataract that has material basis in variation in the region 19q13.

Also known as: CATCN1, CTRCT35, cataract 35, cataract type 35, cataract, congenital nuclear, autosomal recessive 1

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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