|
DOID:0111011 - cone-rod dystrophy 6
Disease Ontology Definition:A cone-rod dystrophy that has_material_basis_in heterozygous mutation in the GUCY2D gene on chromosome 17p13.1.
Synonyms: CORD6, RCD2, retinal cone dystrophy 2,
Echinobase Genes :
MIM:601777 - cone-rod dystrophy 6; cord6 |
Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s):
cone-rod dystrophy (is_a)