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Cataract 13 with adult I phenotype

MONDO:0007289

A cataract that has material basis in homozygous or compound heterozygous mutation in the GCNT2 gene on chromosome 6p24.

Also known as: CTRCT13, cataract 13 with adult I phenotype, cataract 13 with ADULT I phenotype

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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