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1 OMIM reference -
1 associated gene
No signs/symptoms info
COMMON GENES: 1
PROTEIN INTERACTIONS: 2
16 OMIM references -
4 associated genes
No signs/symptoms info
Hereditary cerebral hemorrhage with amyloidosis, Flemish type
Early-onset autosomal dominant Alzheimer disease

APP APP
PSEN1
PSEN2
SORL1


COMMON
GENES
APP


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
APP
APP
(0.88)
(0.84)
PSEN1
PSEN2



Citations in the biomedical literature:


Hereditary cerebral hemorrhage with amyloidosis, Flemish type
APP
Early-onset autosomal dominant Alzheimer disease
PSEN1 PSEN2 SORL1



Hereditary cerebral hemorrhage with amyloidosis, Flemish type
Early-onset autosomal dominant Alzheimer disease

Synonym(s):
- HCHWA, Flemish type

Synonym(s):
- EOFAD
- Early-onset familial autosomal dominant Alzheimer disease
- Familial Alzheimer disease

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

Classification (ICD10):
(no data available)
Classification (ICD10):
- Diseases of the nervous system -

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

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

No signs/symptoms info available.