ODCs

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1 OMIM reference -
1 associated gene
No signs/symptoms info

COMMON GENES: 1
PROTEIN INTERACTIONS: 2

4 associated genes
No signs/symptoms info

Xeroderma pigmentosum complementation group B

Trichothiodystrophy


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
	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 -

	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)

	External references: 1 OMIM reference - No MeSH references		External references: No OMIM references 2 MeSH references: C536559 / D054463

No signs/symptoms info available.