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
Hereditary fructose intolerance

APP ALDOB


INTERACTOME
ASSOCIATIONS

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



Citations in the biomedical literature:


Hereditary cerebral hemorrhage with amyloidosis, Flemish type
APP
Hereditary fructose intolerance
ALDOB



Hereditary cerebral hemorrhage with amyloidosis, Flemish type
Hereditary fructose intolerance

Synonym(s):
- HCHWA, Flemish type

Synonym(s):
- Hereditary fructose-1-phosphate aldolase deficiency
- Hereditary fructosemia

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

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

Epidemiological data:
(no data available)
Epidemiological data:
Class of prevalence: 1-9 / 100 000
Average age onset: neonatal/infancy
Average age of death: normal
Type of inheritance: autosomal recessive

External references:
1 OMIM reference -
No MeSH references
External references:
1 OMIM reference -
1 MeSH reference: D005633

No signs/symptoms info available.