cranio-facial dystonia Gene Set

Dataset DISEASES Text-mining Gene-Disease Assocation Evidence Scores
Category disease or phenotype associations
Type disease
Description A focal dystonia that is characterized as dystonia that affects the muscles of the head, face, and neck. (Human Disease Ontology, DOID_0050845)
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Genes

8 genes co-occuring with the disease cranio-facial dystonia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

Symbol Name Standardized Value
FOXC2 forkhead box C2 1.56844
THAP1 THAP domain containing, apoptosis associated protein 1 1.41753
CAMP cathelicidin antimicrobial peptide 1.4022
SOX18 SRY (sex determining region Y)-box 18 1.32454
FOXC1 forkhead box C1 1.04167
PTS 6-pyruvoyltetrahydropterin synthase 0.97128
GCH1 GTP cyclohydrolase 1 0.91308
FOXP2 forkhead box P2 0.826999