hemifacial hypoplasia Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Unilateral underdevelopment of the facial tissues, including muscles and bones. (Human Phenotype Ontology, HP_0011332)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0011332
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Genes

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

Symbol Name
SIX5 SIX homeobox 5