Disease #00050

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Official abbreviation	XPB
Name	Xeroderma pigmentosum, group B
OMIM ID	610651
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	-
Individuals reported having this disease	0
Phenotype entries for this disease	0
Associated with 1 gene	ERCC3
Associated tissues	-
Disease features	-
Remarks	-