ODCs

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3 OMIM references -
2 associated genes
No signs/symptoms info

PROTEIN INTERACTIONS: 2

4 associated genes
No signs/symptoms info

Cockayne syndrome type 3

Trichothiodystrophy


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	ERCC6 ERCC6	(0.7) (0.63)	ERCC2 ERCC3

Citations in the biomedical literature:

Cockayne syndrome type 3		Trichothiodystrophy

	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: (no data available)		Epidemiological data: (no data available)

	External references: 3 OMIM references - No MeSH references		External references: No OMIM references 2 MeSH references: C536559 / D054463

No signs/symptoms info available.