Cytoscape Web
Click node...


3 associated genes
No signs/symptoms info
PROTEIN INTERACTIONS: 2
1 OMIM reference -
1 associated gene
No signs/symptoms info
Dedifferentiated liposarcoma
Hereditary cerebral hemorrhage with amyloidosis, Flemish type

CDK4 APP
HMGA2
MDM2


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
CDK4
MDM2
(0.56)
(0.56)
APP
APP



Citations in the biomedical literature:


Dedifferentiated liposarcoma
CDK4 HMGA2 MDM2
Hereditary cerebral hemorrhage with amyloidosis, Flemish type
APP



Dedifferentiated liposarcoma
Hereditary cerebral hemorrhage with amyloidosis, Flemish type

Synonym(s):
- DDLS

Synonym(s):
- HCHWA, Flemish type

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

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

Epidemiological data:
Class of prevalence: unknown
Average age onset: adulthood
Average age of death: adult
Type of inheritance: sporadic
Epidemiological data:
(no data available)

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

No signs/symptoms info available.