A cataract that has material basis in homozygous or compound heterozygous mutation in the GCNT2 gene on chromosome 6p24.
Comprehensive, easy-to-understand information about this condition
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Gene data from MyGene.info • Click to view on NCBI Gene
cataract 32 multiple types
MONDO:0007278
cataract 8 multiple types
MONDO:0007280
cataract 42
MONDO:0007283
cataract 20 multiple types
MONDO:0007284
cataract 6 multiple types
MONDO:0007288
cataract 5 multiple types
MONDO:0007290