|Dataset||HPO Gene-Disease Associations|
|Category||disease or phenotype associations|
|Description||The presence of remnants of a fetal membrane that persist as strands of tissue crossing the pupil. (Human Phenotype Ontology, HP_0009917)|
|Downloads & Tools|
3 genes associated with the persistent pupillary membrane phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.