peters' anomaly Gene Set

Dataset GAD Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description A form of anterior segment dysgenesis in which abnormal cleavage of the anterior chamber occurs. Peters anomaly is characterized by central, paracentral, or complete corneal opacity. (Human Phenotype Ontology, HP_0000659)
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Genes

1 genes associated with the disease peters' anomaly in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

Symbol Name
PITX2 paired-like homeodomain 2