Term Name:	retinal cone dystrophy 3A
Synonyms:
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.
Ontology:	Human Disease [DOID:0081025]   ( DOID:0081025 )