Term Name:	achromatopsia 2
Synonyms:	ACHM2, RMCH2, rod monochromacy 2, rod monochromatism 2
Definition:	An achromatopsia that has_material_basis_in homozygous or compound heterozygous mutation in the CNGA3 gene on chromosome 2q11.
Ontology:	Human Disease [DOID:0110007]   ( DOID:0110007 )