Search Ontology:
Human Disease

xeroderma pigmentosum group G

Term ID
DOID:0110849
Synonyms
  • xeroderma pigmentosum VII
  • XP group G
  • XP7
  • XPG
Definition
A xeroderma pigmentosum that has_material_basis_in homozygous or compound heterozygous mutation in the ERCC5 gene on chromosome 13q33. https://www.ncbi.nlm.nih.gov/pubmed/11841555
References
Ontology
Human Disease   ( DOID:0110849 )
Relationships
is a type of
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
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