facial diplegia Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Facial diplegia refers to bilateral facial palsy (bilateral facial palsy is much rarer than unilateral facial palsy). (Human Phenotype Ontology, HP_0001349)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0001349
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Genes

10 genes associated with the facial diplegia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
ABCA1 ATP-binding cassette, sub-family A (ABC1), member 1
C12ORF65 chromosome 12 open reading frame 65
DMPK dystrophia myotonica-protein kinase
SLC12A6 solute carrier family 12 (potassium/chloride transporter), member 6
SLC52A3 solute carrier family 52 (riboflavin transporter), member 3
SOST sclerostin
SUCLA2 succinate-CoA ligase, ADP-forming, beta subunit
TK2 thymidine kinase 2, mitochondrial
TPM2 tropomyosin 2 (beta)
TPM3 tropomyosin 3