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DOID:0111023 - cone-rod dystrophy 17
Disease Ontology Definition:A cone-rod dystrophy that has_material_basis_in variation in the chromosome region 10q26.
Synonyms: CORD17,
Xenbase Genes
![Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries](img/icons/info1.png)
MONDO:0014068 - cone-rod dystrophy 17 |
Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s):
cone-rod dystrophy (is_a)