pulverulent cataract Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description A kind of congenital cataract that is characterized by a hollow sphere of punctate opacities involving the fetal nucleus and that usually occurs bilaterally. (Human Phenotype Ontology, HP_0010693)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0010693
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Genes

5 genes associated with the pulverulent cataract phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
BEST1 bestrophin 1
FTL ferritin, light polypeptide
GJA8 gap junction protein, alpha 8, 50kDa
HSF4 heat shock transcription factor 4
MAF v-maf avian musculoaponeurotic fibrosarcoma oncogene homolog