retinal cone dystrophy 3A (DOID:0081025)
Alliance: disease page
Alt IDs: OMIM:610024, MESH:C566483
Definition: A cone dystrophy that is characterized by reduced visual acuity, photoaversion, night blindness, and abnormal color vision and that has_material_basis_in mutation in the gene encoding the gamma subunit of cone cGMP-phosphodiesterase (PDE6H0) on chromosome 12p13.