mandibulofacial dysostosis Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description OMIM mapping confirmed by DO. [SN]. (Human Disease Ontology, DOID_2908)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0005321
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Genes

2 genes associated with the mandibulofacial dysostosis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
EFTUD2 elongation factor Tu GTP binding domain containing 2
POLR1C polymerase (RNA) I polypeptide C, 30kDa