Disease #00060 (XPB (XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP B), OMIM:610651)

Official abbreviation	XPB
Name	XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP B
OMIM ID	610651
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal recessive
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 3 genes	ERCC3, INS, XPC
Associated tissues	-
Disease features	-
Remarks	-
Date created	2023-06-12 11:32:13 +00:00 (UTC)
Date last edited	N/A

MVZ für Humangenetik Regensburg