persistent pupillary membrane Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description The presence of remnants of a fetal membrane that persist as strands of tissue crossing the pupil. (Human Phenotype Ontology, HP_0009917)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0009917
Similar Terms
Downloads & Tools

Genes

3 genes associated with the persistent pupillary membrane phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
ADAMTSL4 ADAMTS-like 4
ATOH7 atonal homolog 7 (Drosophila)
POMT2 protein-O-mannosyltransferase 2