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2 OMIM references -
3 associated genes
No signs/symptoms info
PROTEIN INTERACTIONS: 1
1 OMIM reference -
1 associated gene
No signs/symptoms info
Cockayne syndrome type 2
Osteosarcoma

ERCC1 CHEK2
ERCC6
ERCC8


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
ERCC6
(0.52)
CHEK2



Citations in the biomedical literature:


Cockayne syndrome type 2
ERCC1 ERCC6 ERCC8
Osteosarcoma
CHEK2



Cockayne syndrome type 2
Osteosarcoma

Synonym(s):
(no synonyms)

Synonym(s):
- Osteogenic sarcoma

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 bone disease
- Rare oncologic disease

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

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:
1 OMIM reference -
1 MeSH reference: D012516

No signs/symptoms info available.