Complementation Group B Xeroderma Pigmentosum

mutation in ERCC3 excision repair gene, which is also found in Cockayne syndrome

Also Known As:

Xeroderma Pigmentosum, Complementation Group B; Xeroderma Pigmentosum, Group B

Neoplasms: 1361496
- Precancerous Conditions: 308
  - Xeroderma Pigmentosum: 1877
    - Complementation Group B Xeroderma Pigmentosum: 23
Congenital, Hereditary, and Neonatal Diseases and Abnormalities: 960
- Congenital Abnormalities: 26404
  - Skin Abnormalities: 159
    - Xeroderma Pigmentosum: 1877
      - Complementation Group B Xeroderma Pigmentosum: 23
- Inborn Genetic Diseases: 12342
  - Genetic Skin Diseases: 51
    - Xeroderma Pigmentosum: 1877
      - Complementation Group B Xeroderma Pigmentosum: 23
Skin and Connective Tissue Diseases
- Skin Diseases: 13402
  - Photosensitivity Disorders: 2774
    - Xeroderma Pigmentosum: 1877
      - Complementation Group B Xeroderma Pigmentosum: 23
  - Skin Abnormalities: 159
    - Xeroderma Pigmentosum: 1877
      - Complementation Group B Xeroderma Pigmentosum: 23
  - Pigmentation Disorders: 152
    - Xeroderma Pigmentosum: 1877
      - Complementation Group B Xeroderma Pigmentosum: 23
  - Genetic Skin Diseases: 51
    - Xeroderma Pigmentosum: 1877
      - Complementation Group B Xeroderma Pigmentosum: 23
Nutritional and Metabolic Diseases: 15
- Metabolic Diseases: 10634
  - DNA Repair-Deficiency Disorders: 544
    - Xeroderma Pigmentosum: 1877
      - Complementation Group B Xeroderma Pigmentosum: 23

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A Cleynen Research Topics