macular dystrophy Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Macular dystrophy is a nonspecific term for premature retinal cell aging and cell death, generally confied to the macula in which no clear extrinsic cause is evident. (Human Phenotype Ontology, HP_0007754)
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4 genes associated with the macular dystrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
CDH3 cadherin 3, type 1, P-cadherin (placental)
ELOVL4 ELOVL fatty acid elongase 4
PROM1 prominin 1
TIMP3 TIMP metallopeptidase inhibitor 3