Choroidal dystrophy central areolar Gene Set

Dataset CTD Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description OMIM mapping confirmed by DO. [SN]. (Human Disease Ontology, DOID_9822)
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1 genes/proteins associated with the disease Choroidal dystrophy central areolar from the curated CTD Gene-Disease Associations dataset.

Symbol Name Standardized Value
CACD central areolar choroidal dystrophy 2.88009