Fleck corneal dystrophy Gene Set

Dataset ClinVar Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description Fleck corneal dystrophy (FCD) is a rare generally asymptomatic form of stromal corneal dystrophy (see this term) characterized by multiple asymptomatic, non-progressive opacities disseminated throughout the corneal stroma with no effect on visual acuity. (Orphanet Rare Disease Ontology, Orphanet_98970)
External Link http://www.omim.org/entry/121850
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1 genes associated with the Fleck corneal dystrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Symbol Name
PIKFYVE phosphoinositide kinase, FYVE finger containing