Respiratory Paralysis Gene Set

Dataset CTD Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description Inability to move the muscles of respiration. (Human Phenotype Ontology, HP_0002203)
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3 genes/proteins associated with the disease Respiratory Paralysis from the curated CTD Gene-Disease Associations dataset.

Symbol Name Standardized Value
TNF tumor necrosis factor 1.19966
FOS FBJ murine osteosarcoma viral oncogene homolog 1.03678
CASP3 caspase 3, apoptosis-related cysteine peptidase 1.01137