has material basis in autosomal dominant disease cataract 1 multiple types A cataract that has_material_basis_in heterozygous mutation in the gene encoding the alpha-8 subunit of the gap junction protein (GJA8) on chromosome 1q21. CAE1 disease_ontology CTRCT1 CZP1 MIM:116200 DOID:0110231 Duffy linked cataract ICD10CM:Q12.0 cataract 1, multiple types, with or without microcornea zonular pulverulent cataract 1 cataract autosomal dominant inheritance