infant botulism Gene Set

Dataset DISEASES Text-mining Gene-Disease Association Evidence Scores
Category disease or phenotype associations
Type disease
Description A botulism that involves intoxication caused by botulinum neurotoxins (BoNTA or B) in infants, has_material_basis_in Clostridium botulinum A or has_material_basis_in Clostridium botulinum B, which are transmitted_by ingestion of bacterial spores, which then grow in the intestine and release toxins. The infection has_symptom constipation, has_symptom lethargy, has_symptom difficulty feeding, has_symptom swallowing, has_symptom ptosis, has_symptom loss of head control, and has_symptom muscle weakness. (Human Disease Ontology, DOID_0050354)
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Genes

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

Symbol Name Standardized Value
SYT2 synaptotagmin II 2.41086
FBXW2 F-box and WD repeat domain containing 2 1.69905
LY96 lymphocyte antigen 96 1.26037
VAMP2 vesicle-associated membrane protein 2 (synaptobrevin 2) 1.21912
SYT1 synaptotagmin I 1.21132
RARA retinoic acid receptor, alpha 0.630813
TYMP thymidine phosphorylase 0.613183
NKX2-1 NK2 homeobox 1 0.607714
NTS neurotensin 0.595233
AVP arginine vasopressin 0.407545