xeroderma pigmentosum Gene Set

Dataset	DISEASES Curated Gene-Disease Association Evidence Scores
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)
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Genes

8 genes involed in the disease xeroderma pigmentosum from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

Symbol	Name
DDB2	damage-specific DNA binding protein 2, 48kDa
ERCC2	excision repair cross-complementation group 2
ERCC3	excision repair cross-complementation group 3
ERCC4	excision repair cross-complementation group 4
ERCC5	excision repair cross-complementation group 5
POLH	polymerase (DNA directed), eta
XPA	xeroderma pigmentosum, complementation group A
XPC	xeroderma pigmentosum, complementation group C