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Summary Literature (1)
OMIM:216900 - ACHROMATOPSIA 2; ACHM2


Xenbase Genes: cnga3

Human Disease Resource: OMIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0009003 - achromatopsia 2

Disease Ontology (DO):
DOID:0110007 - achromatopsia 2