Paraparesis Gene Set

Dataset CTD Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description Weakness or partial paralysis in the lower limbs. (Human Phenotype Ontology, HP_0002385)
External Link http://ctdbase.org/detail.go?type=disease&acc=MESH:D020335
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Genes

1 genes/proteins associated with the disease Paraparesis from the curated CTD Gene-Disease Associations dataset.

Symbol Name Standardized Value
CASP3 caspase 3, apoptosis-related cysteine peptidase 1.12391