Term Name:	cone-rod dystrophy 16
Synonyms:	CORD16, retinal dystrophy with early macular involvement
Definition:	A cone-rod dystrophy that has_material_basis_in homozygous or compound heterozygous mutation in the C8ORF37 gene on chromosome 8q22.
Ontology:	Human Disease [DOID:0111022]   ( DOID:0111022 )