Cytoscape Web
Click node...


1 OMIM reference -
1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
3 associated genes
No signs/symptoms info
Hereditary cerebral hemorrhage with amyloidosis, Flemish type
Multiple acyl-CoA dehydrogenation deficiency, mild type

APP ETFA
ETFB
ETFDH


INTERACTOME
ASSOCIATIONS

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



Citations in the biomedical literature:


Hereditary cerebral hemorrhage with amyloidosis, Flemish type
APP
Multiple acyl-CoA dehydrogenation deficiency, mild type
ETFA ETFB ETFDH



Hereditary cerebral hemorrhage with amyloidosis, Flemish type
Multiple acyl-CoA dehydrogenation deficiency, mild type

Synonym(s):
- HCHWA, Flemish type

Synonym(s):
(no synonyms)

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
- Rare neurologic disease

Classification (ICD10):
(no data available)
Classification (ICD10):
(no data available)

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

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

No signs/symptoms info available.