ODCs

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4 associated genes
No signs/symptoms info

PROTEIN INTERACTIONS: 2

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

Trichothiodystrophy

Cockayne syndrome type 3


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

Citations in the biomedical literature:

Trichothiodystrophy		Cockayne syndrome type 3

	Classification (Orphanet): - Rare developmental defect during embryogenesis - Rare genetic disease - Rare infertility - Rare skin disease		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): - Diseases of the skin and subcutaneous tissue -		Classification (ICD10): - Congenital malformations, deformations and chromosomal abnormalities -

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

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

No signs/symptoms info available.