Term Name: congenital nystagmus 2
Synonyms: autosomal dominant congenital nystagmus 2, congenital motor nystagmus 2, NYS2
Definition: A congenital nystagmus that has_material_basis_in heterozygous mutation in a region of chromosome 6p12.
Ontology: Human Disease [DOID:0111792]   ( DOID:0111792 )

Relationships
is a type of: autosomal dominant disease congenital nystagmus