Term Name: cone-rod dystrophy 24
Synonyms:
Definition: A cone-rod dystrophy that is characterized by night blindness, defective color vision, and reduced visual acuity and that has_material_basis_in heterozygous mutation in the UNC119 gene on chromosome 17q11.
Ontology: Human Disease [DOID:0081449]   ( DOID:0081449 )

Relationships
is a type of: autosomal dominant disease cone-rod dystrophy