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Summary Literature (0)
MIM:278730 - XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP D; XPD

Xenbase Genes: ercc2

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0010212 - laryngeal apparatus
MONDO:0016354 - xeroderma pigmentosum-Cockayne syndrome complex
MONDO:0019600 - xeroderma pigmentosum

Disease Ontology (DO):
DOID:0110845 - xeroderma pigmentosum group D