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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
Glycogen storage disease due to muscle and heart glycogen synthase deficiency

APP GYS1


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
APP
(0.56)
GYS1



Citations in the biomedical literature:


Hereditary cerebral hemorrhage with amyloidosis, Flemish type
APP
Glycogen storage disease due to muscle and heart glycogen synthase deficiency
GYS1



Hereditary cerebral hemorrhage with amyloidosis, Flemish type
Glycogen storage disease due to muscle and heart glycogen synthase deficiency

Synonym(s):
- HCHWA, Flemish type

Synonym(s):
- GSD due to muscle and heart glycogen synthase deficiency
- GSD type 0b
- Glycogen storage disease type 0b
- Glycogenosis due to muscle and heart glycogen synthase deficiency
- Glycogenosis type 0b

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

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

Epidemiological data:
(no data available)
Epidemiological data:
Class of prevalence: <1 / 1 000 000
Average age onset: childhood
Average age of death: child / adolescent
Type of inheritance: sporadic

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

No signs/symptoms info available.