| Term Name: | cataract 47 |
|---|---|
| Synonyms: | CTRCT47 |
| Definition: | A cataract that has_material_basis_in heterozygous mutation in the SLC16A12 gene on chromosome 10q23, characterized by progressive juvenile cataract with microcornea. |
| Ontology: | Human Disease [DOID:0070353] ( DOID:0070353 ) |