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 2 genes ERCC3, INS
Associated tissues -
Disease features -
Remarks -
Date created 2023-06-12 11:32:13 +00:00 (UTC)
Date last edited N/A

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