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 )

Relationships
is a type of: autosomal dominant disease congenital nystagmus