aplasia/hypoplasia affecting the eyelid Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Absence or underdevelopment of the eyelid. (Human Phenotype Ontology, HP_0011226)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0011226
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Genes

1 genes associated with the aplasia/hypoplasia affecting the eyelid phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
PHGDH phosphoglycerate dehydrogenase