peters anomaly Gene Set

Dataset OMIM Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
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)
External Link http://www.omim.org/entry/604229
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Genes

3 genes associated with the peters anomaly phenotype from the curated OMIM Gene-Disease Associations dataset.

Symbol Name
CYP1B1 cytochrome P450, family 1, subfamily B, polypeptide 1
PAX6 paired box 6
PITX2 paired-like homeodomain 2