central scotoma Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description An area of depressed vision located at the point of fixation and that interferes with central vision. (Human Phenotype Ontology, HP_0000603)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0000603
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9 genes associated with the central scotoma phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
ABCA4 ATP-binding cassette, sub-family A (ABC1), member 4
C12ORF65 chromosome 12 open reading frame 65
CACNA1F calcium channel, voltage-dependent, L type, alpha 1F subunit
MFN2 mitofusin 2
OPA1 optic atrophy 1 (autosomal dominant)
PROM1 prominin 1
RAB28 RAB28, member RAS oncogene family
RBP3 retinol binding protein 3, interstitial
TMEM126A transmembrane protein 126A