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1 OMIM reference -
1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
1 OMIM reference -
3 associated genes
No signs/symptoms info
Hereditary cerebral hemorrhage with amyloidosis, Flemish type
Chronic myeloid leukemia

APP ABL1
BCR
RUNX1


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
APP
(0.66)
ABL1



Citations in the biomedical literature:


Hereditary cerebral hemorrhage with amyloidosis, Flemish type
APP
Chronic myeloid leukemia
ABL1 BCR RUNX1



Hereditary cerebral hemorrhage with amyloidosis, Flemish type
Chronic myeloid leukemia

Synonym(s):
- HCHWA, Flemish type

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

Classification (Orphanet):
- Rare genetic disease
- Rare neurologic disease
- Rare systemic or rheumatologic disease
Classification (Orphanet):
- Rare hematologic disease
- Rare oncologic disease

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

Epidemiological data:
(no data available)
Epidemiological data:
Class of prevalence: 1-9 / 100 000
Average age onset: adulthood
Average age of death: -
Type of inheritance: sporadic

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

No signs/symptoms info available.