multicentric reticulohistiocytosis Gene Set

Dataset DISEASES Text-mining Gene-Disease Association Evidence Scores
Category disease or phenotype associations
Type disease
Description A rare systemic granulomatous syndrome characterized by papulonodular skin lesions containing a proliferation of true macrophages associated with arthritis. (Human Disease Ontology, DOID_11824)
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Genes

17 genes co-occuring with the disease multicentric reticulohistiocytosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

Symbol Name Standardized Value
CD68 CD68 molecule 1.41183
HAVCR1 hepatitis A virus cellular receptor 1 1.1456
LYZ lysozyme 1.00583
ACPP acid phosphatase, prostate 0.905675
TNFRSF1B tumor necrosis factor receptor superfamily, member 1B 0.899514
S100A9 S100 calcium binding protein A9 0.889668
ADGRV1 adhesion G protein-coupled receptor V1 0.715618
FUT4 fucosyltransferase 4 (alpha (1,3) fucosyltransferase, myeloid-specific) 0.523816
CD1C CD1c molecule 0.461639
CD34 CD34 molecule 0.4443
TNF tumor necrosis factor 0.439034
CD163 CD163 molecule 0.34384
CTSK cathepsin K 0.33944
IL1B interleukin 1, beta 0.321181
PTPRC protein tyrosine phosphatase, receptor type, C 0.283655
IL6 interleukin 6 0.272953
SEBOX SEBOX homeobox 0.264785