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Summary Literature (0)
MIM:610651 - XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP B; XPB

Xenbase Genes: ercc3

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0012531 - xeroderma pigmentosum group B
MONDO:0016354 - xeroderma pigmentosum-Cockayne syndrome complex
MONDO:0019600 - xeroderma pigmentosum

Disease Ontology (DO):
DOID:0110850 - xeroderma pigmentosum group B