Ectopia pupillae Gene Set

Dataset CTD Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description A malposition of the pupil owing to a developmental defect of the iris. (Human Phenotype Ontology, HP_0009918)
External Link http://ctdbase.org/detail.go?type=disease&acc=MESH:C536185
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Genes

1 genes/proteins associated with the disease Ectopia pupillae from the curated CTD Gene-Disease Associations dataset.

Symbol Name Standardized Value
PAX6 paired box 6 2.88009