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Cone-Rod Dystrophy 6

Disease ID: disease_node_16589

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DbxrefGARD:10656, MIM:601777
SubclassofDOID_0050572
Data SourceDOID
SynonymsCORD6, RCD2, retinal cone dystrophy 2
Doid Labelcone-rod dystrophy 6
Doid DescriptionA cone-rod dystrophy that has_material_basis_in heterozygous mutation in the GUCY2D gene on chromosome 17p13.1.
Disease Node Iddisease_node_16589
Doid IdDOID_0111011
LabelCone-Rod Dystrophy 6