OBO ID: DOID:0110849
Term Name: xeroderma pigmentosum group G Search Ontology:
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 xeroderma pigmentosum group G PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
ERCC5 Xeroderma pigmentosum, group G/Cockayne syndrome 278780
Xeroderma pigmentosum, group G 278780
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None
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