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1 OMIM reference -
1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
2 OMIM references -
5 associated genes
No signs/symptoms info
Hereditary cerebral hemorrhage with amyloidosis, Flemish type
Fatal infantile cytochrome C oxidase deficiency

APP COX10
COX15
SCO1
SCO2
SURF1


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
APP
(0.56)
SCO2



Citations in the biomedical literature:


Hereditary cerebral hemorrhage with amyloidosis, Flemish type
APP
Fatal infantile cytochrome C oxidase deficiency
COX10 COX15 SCO1 SCO2 SURF1



Hereditary cerebral hemorrhage with amyloidosis, Flemish type
Fatal infantile cytochrome C oxidase deficiency

Synonym(s):
- HCHWA, Flemish type

Synonym(s):
- Fatal infantile COX deficiency
- Fatal infantile cardioencephalomyopathy due to cytochrome c oxidase deficiency

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

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

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

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

No signs/symptoms info available.