| Term Name: | cataract 13 with adult i phenotype |
|---|---|
| Synonyms: | CTRCT13 |
| Definition: | A cataract that has_material_basis_in homozygous or compound heterozygous mutation in the GCNT2 gene on chromosome 6p24. |
| Ontology: | Human Disease [DOID:0110242] ( DOID:0110242 ) |