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1 OMIM reference -
1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
Hereditary cerebral hemorrhage with amyloidosis, Flemish type
Adult-onset multiple mitochondrial DNA deletion syndrome due to DGUOK deficiency

APP DGUOK


INTERACTOME
ASSOCIATIONS

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



Citations in the biomedical literature:


Hereditary cerebral hemorrhage with amyloidosis, Flemish type
APP
Adult-onset multiple mitochondrial DNA deletion syndrome due to DGUOK deficiency
DGUOK



Hereditary cerebral hemorrhage with amyloidosis, Flemish type
Adult-onset multiple mitochondrial DNA deletion syndrome due to DGUOK deficiency

Synonym(s):
- HCHWA, Flemish type

Synonym(s):
- Adult-onset multiple mtDNA deletion syndrome due to DGUOK deficiency

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

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

Epidemiological data:
(no data available)
Epidemiological data:
Class of prevalence: unknown
Average age onset: adulthood
Average age of death: -
Type of inheritance: autosomal recessive

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

No signs/symptoms info available.