Cytoscape Web
Click node...


1 OMIM reference -
1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
1 OMIM reference -
1 associated gene
No signs/symptoms info
Hereditary cerebral hemorrhage with amyloidosis, Flemish type
Myelodysplastic syndrome associated with isolated del(5q) chromosome abnormality

APP RPS14


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
APP
(0.56)
RPS14



Citations in the biomedical literature:


Hereditary cerebral hemorrhage with amyloidosis, Flemish type
APP
Myelodysplastic syndrome associated with isolated del(5q) chromosome abnormality
RPS14



Hereditary cerebral hemorrhage with amyloidosis, Flemish type
Myelodysplastic syndrome associated with isolated del(5q) chromosome abnormality

Synonym(s):
- HCHWA, Flemish type

Synonym(s):
- 5q- syndrome

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:
(no data available)

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

No signs/symptoms info available.