skeletal tuberculosis Gene Set

Dataset DISEASES Text-mining Gene-Disease Assocation Evidence Scores
Category disease or phenotype associations
Type disease
Description An extrapulmonary tuberculosis that results in formation of lesions located_in bone. (Human Disease Ontology, DOID_1639)
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17 genes co-occuring with the disease skeletal tuberculosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

Symbol Name Standardized Value
ESX1 ESX homeobox 1 1.3062
AMELY amelogenin, Y-linked 0.808539
AMELX amelogenin, X-linked 0.774932
SMUG1 single-strand-selective monofunctional uracil-DNA glycosylase 1 0.720461
NLRP3 NLR family, pyrin domain containing 3 0.572662
CRP C-reactive protein, pentraxin-related 0.493122
F9 coagulation factor IX 0.41727
MRAP melanocortin 2 receptor accessory protein 0.387051
ACTB actin, beta 0.371847
ACTG1 actin gamma 1 0.342372
ADA adenosine deaminase 0.308842
CP ceruloplasmin (ferroxidase) 0.278654
LARGE like-glycosyltransferase 0.277584
HP haptoglobin 0.268687
HPR haptoglobin-related protein 0.263014
MBNL1 muscleblind-like splicing regulator 1 0.213621
LYZ lysozyme 0.195501