|  Help  |  About  |  Contact Us

DO Term : xeroderma pigmentosum group F [DOID:0110848] Disease Ontology

Namespace  disease_ontology Obsolete  false
description  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.
  • synonyms:
  • XP6,
  • OMIM:278760,
  • 278760,
  • xeroderma pigmentosum VI,
  • ICD10CM:Q82.1,
  • XPF,
  • XP group F
Quick Links:
 
Quick Links:
 

Disease

Diseases --> Human genes

Diseases --> Mouse genes

Diseases --> Mouse models

Ontology

Ontology Term --> All ancestors

Ontology Term --> All descendants

Ontology Term --> Direct children

Ontology Term --> Direct parents