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Xeroderma pigmentosum complementation group B
1 OMIM reference -
1 associated gene
27 connected diseases
No signs/symptoms info
Disease Type of connection
Trichothiodystrophy
COFS syndrome
Precursor B-cell acute lymphoblastic leukemia
Precursor T-cell acute lymphoblastic leukemia
UV-sensitive syndrome
Xeroderma pigmentosum complementation group D
Adrenocortical carcinoma
B-cell chronic lymphocytic leukemia
Essential thrombocythemia
Familial pancreatic carcinoma
Giant cell glioblastoma
Gliosarcoma
Li-Fraumeni syndrome
Papilloma of choroid plexus
Chronic myeloid leukemia
Distal 22q11.2 microdeletion syndrome
Xeroderma pigmentosum complementation group G
Xeroderma pigmentosum complementation group C
Complete androgen insensitivity syndrome
Familial hypospadias
Kennedy disease
Partial androgen insensitivity syndrome
Burkitt lymphoma
Cockayne syndrome type 1
Cockayne syndrome type 2
Cockayne syndrome type 3
BOR syndrome
Synonym(s):
- XPB
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
ERCC3 P19447133510
No signs/symptoms info available.