primary amebic meningoencephalitis Gene Set

Dataset DISEASES Text-mining Gene-Disease Assocation Evidence Scores
Category disease or phenotype associations
Type disease
Description A parasitic protozoa infectious disease that involves infection of the central nervous system caused by Naegleria fowleri. The symptoms include headache, nausea, rigidity of the neck muscles, vomiting, delirium, seizures and coma. (Human Disease Ontology, DOID_0050242)
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18 genes co-occuring with the disease primary amebic meningoencephalitis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

Symbol Name Standardized Value
C9 complement component 9 1.41621
HM13 histocompatibility (minor) 13 1.13374
AOX1 aldehyde oxidase 1 1.10678
SULT1E1 sulfotransferase family 1E, estrogen-preferring, member 1 1.02903
CD59 CD59 molecule, complement regulatory protein 0.937044
XDH xanthine dehydrogenase 0.88434
MDH2 malate dehydrogenase 2, NAD (mitochondrial) 0.788852
MDH1 malate dehydrogenase 1, NAD (soluble) 0.772887
CTSL cathepsin L 0.678302
GPI glucose-6-phosphate isomerase 0.675112
STAT6 signal transducer and activator of transcription 6, interleukin-4 induced 0.59952
LAP3 leucine aminopeptidase 3 0.57655
IDH2 isocitrate dehydrogenase 2 (NADP+), mitochondrial 0.553627
IDH1 isocitrate dehydrogenase 1 (NADP+), soluble 0.513802
CD69 CD69 molecule 0.477909
G6PD glucose-6-phosphate dehydrogenase 0.37629
CD79A CD79a molecule, immunoglobulin-associated alpha 0.243995
JUN jun proto-oncogene 0.201308