melkersson-rosenthal syndrome Gene Set

Dataset DISEASES Text-mining Gene-Disease Association Evidence Scores
Category disease or phenotype associations
Type disease
Description OMIM mapping confirmed by DO. [SN]. (Human Disease Ontology, DOID_1761)
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Genes

11 genes co-occuring with the disease melkersson-rosenthal syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

Symbol Name Standardized Value
UNC93B1 unc-93 homolog B1 (C. elegans) 1.31493
PTPRN2 protein tyrosine phosphatase, receptor type, N polypeptide 2 1.04462
LALBA lactalbumin, alpha- 0.906909
NR1I2 nuclear receptor subfamily 1, group I, member 2 0.805257
ACE angiotensin I converting enzyme 0.61866
SERPING1 serpin peptidase inhibitor, clade G (C1 inhibitor), member 1 0.594454
CD4 CD4 molecule 0.304503
TNFRSF1B tumor necrosis factor receptor superfamily, member 1B 0.255946
LYZ lysozyme 0.255241
MMP2 matrix metallopeptidase 2 0.182375
ALB albumin 0.165874