Search Ontology:
Human Disease

xeroderma pigmentosum group B

Term ID
DOID:0110850
Synonyms
  • XP group B
  • XPB
  • XPBC
Definition
A xeroderma pigmentosum characterized by that has_material_basis_in mutation in the ERCC3 gene on chromosome 2q14. https://www.ncbi.nlm.nih.gov/pubmed/16947863
References
Ontology
Human Disease   ( DOID:0110850 )
Relationships
is a type of
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
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