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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