ODCs

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

COMMON GENES: 2
PROTEIN INTERACTIONS: 1

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

Cockayne syndrome type 2

Cockayne syndrome type 3


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	ERCC6	(0.89)	ERCC8

Citations in the biomedical literature:

Cockayne syndrome type 2		Cockayne syndrome type 3

	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 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 -		Classification (ICD10): - Congenital malformations, deformations and chromosomal abnormalities -

	Epidemiological data: Class of prevalence: - Average age onset: - Average age of death: - Type of inheritance: autosomal recessive		Epidemiological data: (no data available)

	External references: 2 OMIM references - No MeSH references		External references: 3 OMIM references - No MeSH references

No signs/symptoms info available.