Search Ontology:
Human Disease

xeroderma pigmentosum group F

Term ID
DOID:0110848
Synonyms
  • xeroderma pigmentosum VI
  • XP group F
  • XP6
  • XPF
Definition
A xeroderma pigmentosum characterized by milder symptoms and later onset of skin cancer that has_material_basis_in homozygous or compound heterozygous mutation in the ERCC4 gene on chromosome 16p13. (2)
References
Ontology
Human Disease   ( DOID:0110848 )
Relationships
is a type of
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
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