fish-eye disease Gene Set

Dataset OMIM Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Fish eye disease (FED) is a form of genetic LCAT (lecithin-cholesterol acyltransferase) deficiency (see this term) characterized clinically by corneal opacifications, and biochemically by significantly reduced HDL cholesterol and partial LCAT enzyme deficiency. (Orphanet Rare Disease Ontology, Orphanet_79292)
External Link http://www.omim.org/entry/136120
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Genes

1 genes associated with the fish-eye disease phenotype from the curated OMIM Gene-Disease Associations dataset.

Symbol Name
LCAT lecithin-cholesterol acyltransferase