Paraplegia Gene Set

Dataset CTD Gene-Disease Associations
Category disease or phenotype associations
Type disease
External Link http://ctdbase.org/detail.go?type=disease&acc=MESH:D010264
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Genes

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

Symbol Name Standardized Value
SPG7 spastic paraplegia 7 (pure and complicated autosomal recessive) 2.88009
CASP3 caspase 3, apoptosis-related cysteine peptidase 1.52489
BCL2 B-cell CLL/lymphoma 2 1.38891
BAX BCL2-associated X protein 1.20622
PRL prolactin 1.19542
FAS Fas cell surface death receptor 1.09401