| Term Name: | congenital nystagmus 7 |
|---|---|
| Synonyms: | autosomal dominant congenital nystagmus 7, NYS7 |
| Definition: | A congenital nystagmus that has_material_basis_in heterozygous mutation in a region of chromosome 1q31.3-q32.1. |
| Ontology: | Human Disease [DOID:0111791] ( DOID:0111791 ) |