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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
MEGDEL syndrome

APP SERAC1


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
APP
(0.56)
SERAC1



Citations in the biomedical literature:


Hereditary cerebral hemorrhage with amyloidosis, Flemish type
APP
MEGDEL syndrome
SERAC1



Hereditary cerebral hemorrhage with amyloidosis, Flemish type
MEGDEL syndrome

Synonym(s):
- HCHWA, Flemish type

Synonym(s):
- 3-methylglutaconic aciduria with deafness - encephalopathy - Leigh-like syndrome

Classification (Orphanet):
- Rare genetic disease
- Rare neurologic disease
- Rare systemic or rheumatologic disease
Classification (Orphanet):
- Inborn errors of metabolism
- Rare developmental defect during embryogenesis
- Rare genetic disease
- Rare neurologic disease
- Rare otorhinolaryngologic 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: neonatal/infancy
Average age of death: -
Type of inheritance: autosomal recessive

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

No signs/symptoms info available.