acute hemorrhagic leukoencephalitis Gene Set

Dataset DISEASES Text-mining Gene-Disease Assocation Evidence Scores
Category disease or phenotype associations
Type disease
Description A very rare form of acute disseminated encephalomyelitis, characterized by a brief but intense attack of inflammation and necrotizing vasculitis of venules and hemorrhage, and edema. (Human Disease Ontology, DOID_10992)
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Genes

12 genes co-occuring with the disease acute hemorrhagic leukoencephalitis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

Symbol Name Standardized Value
NRP1 neuropilin 1 1.2508
CFI complement factor I 1.11435
PRF1 perforin 1 (pore forming protein) 0.862637
AQP1 aquaporin 1 (Colton blood group) 0.859771
OCLN occludin 0.630027
AQP4 aquaporin 4 0.502675
MBP myelin basic protein 0.498849
TNFRSF1A tumor necrosis factor receptor superfamily, member 1A 0.480945
IL1RN interleukin 1 receptor antagonist 0.42289
FLT1 fms-related tyrosine kinase 1 0.402692
FASLG Fas ligand (TNF superfamily, member 6) 0.355235
TNFRSF1B tumor necrosis factor receptor superfamily, member 1B 0.266913