Paresis Gene Set

Dataset HuGE Navigator Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description partial loss of power of voluntary movement in a muscle through injury or disease of it or its nerve supply (Mammalian Phenotype Ontology, MP_0000754)
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4 genes associated with the Paresis phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Symbol Name
BDNF brain-derived neurotrophic factor
F2 coagulation factor II (thrombin)
F5 coagulation factor V (proaccelerin, labile factor)
MTHFR methylenetetrahydrofolate reductase (NAD(P)H)