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Xeroderma pigmentosum complementation group F
1 OMIM reference -
1 associated gene
12 connected diseases
No signs/symptoms info
Disease Type of connection
Fanconi anemia
Cockayne syndrome type 1
COFS syndrome
Cockayne syndrome type 2
Hereditary spherocytosis
Cockayne syndrome type 3
Constitutional mismatch repair deficiency syndrome
Hereditary nonpolyposis colon cancer
Muir-Torre syndrome
Non-polyposis Turcot syndrome
UV-sensitive syndrome
Xeroderma pigmentosum complementation group C
Synonym(s):
- XPF
Classification (Orphanet):
- Rare developmental defect during embryogenesis
- Rare eye disease
- Rare genetic disease
- Rare neurologic disease
- Rare oncologic disease
- Rare otorhinolaryngologic disease
- Rare skin disease
Classification (ICD10):
- Congenital malformations, deformations and chromosomal abnormalities -
Epidemiological data:
Class of prevalence: <1 / 1 000 000
Average age onset: variable
Average age of death: -
Type of inheritance: autosomal recessive
External references:
1 OMIM reference -
No MeSH references
Gene symbol UniProt reference OMIM reference
ERCC4 Q92889133520
No signs/symptoms info available.