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 |
- |
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