Xeroderma Pigmentosum Gene Set

Dataset CTD Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description An autosomal recessive disease that is characterized by a deficiency in the ability to repair ultraviolet damage that has_material_basis_in autosomal recessive inheritance of DNA repair. (Human Disease Ontology, DOID_0050427)
External Link http://ctdbase.org/detail.go?type=disease&acc=MESH:D014983
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Genes

2 genes/proteins associated with the disease Xeroderma Pigmentosum from the curated CTD Gene-Disease Associations dataset.

Symbol Name Standardized Value
POLH polymerase (DNA directed), eta 2.88009
XPA xeroderma pigmentosum, complementation group A 2.88009