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1 OMIM reference -
3 associated genes
No signs/symptoms info
PROTEIN INTERACTIONS: 2
1 associated gene
No signs/symptoms info
Chronic myeloid leukemia
Familial retinoblastoma

ABL1 RB1
BCR
RUNX1


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
ABL1
BCR
(0.9)
(0.72)
RB1
RB1



Citations in the biomedical literature:


Chronic myeloid leukemia
ABL1 BCR RUNX1
Familial retinoblastoma
RB1



Chronic myeloid leukemia
Familial retinoblastoma

Synonym(s):
- Chronic granulocytic leukemia
- Chronic myelogenous leukemia

Synonym(s):
- Bilateral retinoblastoma
- Hereditary retinoblastoma

Classification (Orphanet):
- Rare hematologic disease
- Rare oncologic disease
Classification (Orphanet):
- Rare eye disease
- Rare genetic disease
- Rare oncologic disease

Classification (ICD10):
- Neoplasms -
Classification (ICD10):
- Neoplasms -

Epidemiological data:
Class of prevalence: 1-9 / 100 000
Average age onset: adulthood
Average age of death: -
Type of inheritance: sporadic
Epidemiological data:
Class of prevalence: unknown
Average age onset: neonatal/infancy
Average age of death: any age
Type of inheritance: autosomal dominant

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

No signs/symptoms info available.