Term Name: xeroderma pigmentosum group F
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.
Ontology: Human Disease [DOID:0110848]   ( DOID:0110848 )

Relationships
is a type of: xeroderma pigmentosum