common wart Gene Set

Dataset DISEASES Text-mining Gene-Disease Association Evidence Scores
Category disease or phenotype associations
Type disease
Description A viral infectious disease that results_in infection located_in skin, has_material_basis_in human papillomavirus (types 2 and 4). This infection has_symptom raised wart with roughened surface, most common on hands, but can grow anywhere on the body. (Human Disease Ontology, DOID_11165)
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Genes

10 genes co-occuring with the disease common wart in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

Symbol Name Standardized Value
CLEC6A C-type lectin domain family 6, member A 1.63142
CLEC4E C-type lectin domain family 4, member E 1.5818
MRC1 mannose receptor, C type 1 0.9717
NFIC nuclear factor I/C (CCAAT-binding transcription factor) 0.940364
NFIX nuclear factor I/X (CCAAT-binding transcription factor) 0.937874
CD209 CD209 molecule 0.91061
LGALS3 lectin, galactoside-binding, soluble, 3 0.6214
CD80 CD80 molecule 0.499614
CD40 CD40 molecule, TNF receptor superfamily member 5 0.413527
CD4 CD4 molecule 0.278654