Term Name:	cone-rod dystrophy 6
Synonyms:	CORD6, RCD2, retinal cone dystrophy 2
Definition:	A cone-rod dystrophy that has_material_basis_in heterozygous mutation in the GUCY2D gene on chromosome 17p13.1.
Ontology:	Human Disease [DOID:0111011]   ( DOID:0111011 )