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1 OMIM reference -
1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
1 OMIM reference -
4 associated genes
No signs/symptoms info
Osteosarcoma
Constitutional mismatch repair deficiency syndrome

CHEK2 MLH1
MSH2
MSH6
PMS2


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
CHEK2
(0.89)
MSH2



Citations in the biomedical literature:


Osteosarcoma
CHEK2
Constitutional mismatch repair deficiency syndrome
MLH1 MSH2 MSH6 PMS2



Osteosarcoma
Constitutional mismatch repair deficiency syndrome

Synonym(s):
- Osteogenic sarcoma

Synonym(s):
- CMMR-D syndrome

Classification (Orphanet):
- Rare bone disease
- Rare oncologic disease
Classification (Orphanet):
- Rare genetic disease
- Rare neurologic disease
- Rare oncologic disease

Classification (ICD10):
- Neoplasms -
Classification (ICD10):
(no data available)

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

External references:
1 OMIM reference -
1 MeSH reference: D012516
External references:
1 OMIM reference -
No MeSH references

No signs/symptoms info available.