subcapsular cataract Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description A cataract that affects the region of the lens directly beneath the capsule of the lens. (Human Phenotype Ontology, HP_0000523)
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13 genes associated with the subcapsular cataract phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
ABHD12 abhydrolase domain containing 12
ABHD5 abhydrolase domain containing 5
ADAMTS18 ADAM metallopeptidase with thrombospondin type 1 motif, 18
ALMS1 Alstrom syndrome protein 1
CHMP4B charged multivesicular body protein 4B
CNBP CCHC-type zinc finger, nucleic acid binding protein
FZD4 frizzled class receptor 4
IMPG2 interphotoreceptor matrix proteoglycan 2
LRP5 low density lipoprotein receptor-related protein 5
NF2 neurofibromin 2 (merlin)
OAT ornithine aminotransferase
OFD1 oral-facial-digital syndrome 1
RBP3 retinol binding protein 3, interstitial