Cytoscape Web
Click node...


1 OMIM reference -
1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
1 OMIM reference -
4 associated genes
No signs/symptoms info
Hereditary cerebral hemorrhage with amyloidosis, Flemish type
Hyperlipoproteinemia type 5

APP APOA5
CREB3L3
GPIHBP1
LPL


INTERACTOME
ASSOCIATIONS

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



Citations in the biomedical literature:


Hereditary cerebral hemorrhage with amyloidosis, Flemish type
APP
Hyperlipoproteinemia type 5
APOA5 CREB3L3 GPIHBP1 LPL



Hereditary cerebral hemorrhage with amyloidosis, Flemish type
Hyperlipoproteinemia type 5

Synonym(s):
- HCHWA, Flemish type

Synonym(s):
- Major hyperlipidemia

Classification (Orphanet):
- Rare genetic disease
- Rare neurologic disease
- Rare systemic or rheumatologic disease
Classification (Orphanet):
- Inborn errors of metabolism
- Rare endocrine disease
- Rare genetic disease

Classification (ICD10):
(no data available)
Classification (ICD10):
- Endocrine, nutritional and metabolic diseases -

Epidemiological data:
(no data available)
Epidemiological data:
(no data available)

External references:
1 OMIM reference -
No MeSH references
External references:
1 OMIM reference -
1 MeSH reference: D006954

No signs/symptoms info available.