. "A cataract that has_material_basis_in homozygous or compound heterozygous mutation in the GCNT2 gene on chromosome 6p24."^^ . "disease_ontology"^^ . . _:vb50942766 . . _:vb50942766 . _:vb50942766 . "OMIM:116700"^^ . "CTRCT13"@en . . _:vb50942766 . "DOID:0110242"^^ . "ICD10CM:Q12.0"^^ . "cataract 13 with adult i phenotype"^^ . _:vb50942766 .