Human genes for congenital nystagmus 2
Congenital nystagmus 2 [DOID:0111792]
A congenital nystagmus that has_material_basis_in heterozygous mutation in a region of chromosome 6p12.
Synonyms: congenital nystagmus 2, DOID:0111792, autosomal dominant congenital nystagmus 2, congenital motor nystagmus 2, NYS2