Xeroderma pigmentosum complementation group B |
Trichothiodystrophy |
ERCC3 | ERCC2 | |||
ERCC3 | ||||
GTF2H5 | ||||
MPLKIP |
COMMON GENES |
ERCC3 |
INTERACTOME ASSOCIATIONS (click on a score value to see the evidence) |
ERCC3 ERCC3 | (0.97) (0.87) | ERCC2 GTF2H5 | |
Citations in the biomedical literature:
Xeroderma pigmentosum complementation group B |
Trichothiodystrophy |
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Synonym(s): - XPB | Synonym(s): (no synonyms) | ||
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 (Orphanet): - Rare developmental defect during embryogenesis - Rare genetic disease - Rare infertility - Rare skin disease | ||
Classification (ICD10): - Congenital malformations, deformations and chromosomal abnormalities -
| Classification (ICD10): - Diseases of the skin and subcutaneous tissue -
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Epidemiological data: Class of prevalence: <1 / 1 000 000 Average age onset: variable Average age of death: - Type of inheritance: autosomal recessive | Epidemiological data: (no data available)
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External references: 1 OMIM reference -
No MeSH references | External references: No OMIM references 2 MeSH references: C536559 / D054463 | ||