Disease #00985 (XPG (xeroderma pigmentosum, complementation group G (XPG)), OMIM:278780)

Official abbreviation XPG
Name xeroderma pigmentosum, complementation group G (XPG)
OMIM ID 278780
Human Phenotype Ontology Project (HPO) HPO
Inheritance -
Individuals reported having this disease 0
Phenotype entries for this disease 0
Associated with 1 gene ERCC5
Associated tissues -
Disease features -
Remarks -