Disease #00747

Official abbreviation XPD
Name xeroderma pigmentosum, complementation group D (XPD)
OMIM ID 278730
Human Phenotype Ontology Project (HPO) HPO
Inheritance -
Individuals reported having this disease 0
Phenotype entries for this disease 0
Associated with 1 gene ERCC2
Associated tissues -
Disease features -
Remarks -