congenital ptosis Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description A ptosis characterized by eyelid drop present at birth. (Human Disease Ontology, DOID_0060261)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0007970
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Genes

1 genes associated with the congenital ptosis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
ZFHX4 zinc finger homeobox 4