|OBO ID: DOID:0050795|
|Term Name:||cone dystrophy||Search Ontology:|
|Definition:||A retinal disease that is characterized by the loss of cone cells, the photoreceptors responsible for both central and color vision. (3)|
|Ontology:||Human Disease (DOID:0050795)|
OTHER cone dystrophy PAGES
GENES INVOLVED No data available
PHENOTYPE No data available
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